Medlog GmbH Marketing Services: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Medlog GmbH Marketing Services” (first 1981, latest 1983), across 5 product codes in 3 review panels. Median 510(k) review time under this name: 38 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| BTT | Humidifier, Respiratory Gas, (Direct Patient Interface) | 1 | 1 |
| CAF | Nebulizer (Direct Patient Interface) | 1 | 1 |
| FRN | Pump, Infusion | 1 | 1 |
| GBB | Chair, Surgical, Ac-Powered | 1 | 1 |
Plus 1 more product codes.
Review panels
Most recent Medlog GmbH Marketing Services 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K832086 | USE 77 ULTRASONIC NEBULIZER | CAF | 1983-07-19 | 21 |
| K831325 | NUTROMAT | GBB | 1983-06-02 | 38 |
| K830913 | MINITROP AEROSAL, PRODOMO AEROSAL AND | BTT | 1983-05-25 | 65 |
| K813455 | PUMP & DETECTOR | FRN | 1982-01-05 | 36 |
| K810155 | DOP 84 | — | 1981-05-01 | 100 |
Recalls
openFDA lists no recalls under a recalling firm named Medlog GmbH Marketing Services.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Related HCPCS codes
HCPCS Level II codes whose descriptors match the device names of the product codes filed under Medlog GmbH Marketing Services (a text match, not an official crosswalk):
- A4220 — Refill kit for implantable infusion pump (via FRN)
- E0786 — Implantable programmable infusion pump, replacement (excludes implantable intraspinal catheter) (via FRN)
- E0785 — Implantable intraspinal (epidural/intrathecal) catheter used with implantable infusion pump, replacement (via FRN)
- G0379 — Direct admission of patient for hospital observation care (via CAF)
Frequently asked questions
How many FDA 510(k) clearances are listed under Medlog GmbH Marketing Services?
FDA lists 5 510(k) clearances under the applicant name “Medlog GmbH Marketing Services” (first 1981, latest 1983), across 5 product codes in 3 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Medlog GmbH Marketing Services?
The median time from FDA receipt to decision across 510(k)s cleared under the name Medlog GmbH Marketing Services is 38 days.
Which FDA product codes appear under Medlog GmbH Marketing Services?
The most frequent FDA product codes under this applicant name are BTT (Humidifier, Respiratory Gas, (Direct Patient Interface), 1); CAF (Nebulizer (Direct Patient Interface), 1); FRN (Pump, Infusion, 1).
Next steps
- See all 5 Medlog GmbH Marketing Services clearances with predicates and recalls
- Run predicate analysis for product code BTT, Medlog GmbH Marketing Services's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.