FDA product code BRY: Cabinet, Table And Tray, Anesthesia
BRY is the FDA product code for cabinet, table and tray, anesthesia. It is a Class I device, regulated under 21 CFR 868.6100 and reviewed by the Anesthesiology panel. FDA has cleared 5 510(k) submissions under BRY, from 5 different applicants. The average 510(k) review took 39 days (median 26). FDA has posted 99 recalls for BRY devices, 85 initiated in the last five years.
Classification
| Field | Value |
|---|---|
| Device name | Cabinet, Table And Tray, Anesthesia |
| Device class | Class I |
| Regulation | 21 CFR 868.6100 |
| Review panel | AN — Anesthesiology |
| Medical specialty | Anesthesiology |
| Premarket route | 510(k) exempt |
Compare with all 510(k) review times · Search every BRY clearance
Top BRY applicants
| Applicant | Clearances | Latest |
|---|---|---|
| John J. Navar, M.D. | 1 | 1992-06-29 |
| Medikeeper, Inc. | 1 | 1991-07-30 |
| Siemens Life Support Systems | 1 | 1990-04-10 |
| Anestech, Inc. | 1 | 1987-05-18 |
| Med-Life, Inc. | 1 | 1982-05-14 |
Most recent BRY clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K921710 | John J. Navar, M.D. | MOVIT DEVICE | 1992-06-29 | 82 |
| K912346 | Medikeeper, Inc. | MEDIKEEPER | 1991-07-30 | 63 |
| K901474 | Siemens Life Support Systems | ANESTHESIA WORKSTATION | 1990-04-10 | 14 |
| K871564 | Anestech, Inc. | ANESTHASSIST | 1987-05-18 | 26 |
| K821307 | Med-Life, Inc. | ANESTHECACHE | 1982-05-14 | 10 |
Recalls for BRY devices
99 product recalls in 46 recall events; 85 initiated in the last five years and 85 still open. Most recent: 2026-04-30.
| Year | Recalls |
|---|---|
| 2022 | 3 |
| 2023 | 14 |
| 2024 | 38 |
| 2025 | 22 |
| 2026 | 8 |
Frequently asked questions
What is FDA product code BRY?
BRY is the FDA product code for cabinet, table and tray, anesthesia. It is a Class I device, regulated under 21 CFR 868.6100 and reviewed by the Anesthesiology panel.
What device class is BRY?
Class I, regulation 21 CFR 868.6100. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code BRY?
Across 5 cleared submissions the average was 39 days from receipt to decision (median 26).
Which companies have the most BRY clearances?
John J. Navar, M.D. (1); Medikeeper, Inc. (1); Siemens Life Support Systems (1); Anestech, Inc. (1); Med-Life, Inc. (1).
Have BRY devices been recalled?
Yes: 99 product recalls across 46 recall events; the most recent began 2026-04-30.
Next steps
- Run an FDA pathway report with predicate devices for product code BRY
- Run a recall and safety report across every BRY manufacturer
- Watch product code BRY for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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