Datachem, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Datachem, Inc.” (first 1981, latest 1990), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 86 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

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
JJEAnalyzer, Chemistry (Photometric, Discrete), For Clinical Use22
LGZWarmer, Thermal, Infusion Fluid22
CEMElectrode, Ion Specific, Potassium11

Review panels

Most recent Datachem, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K900788MODIFIED APSARA CLINICAL DIAGNOSTIC ANALYZERCEM1990-07-05135
K834534APSARA ANALYZERJJE1984-03-0978
K823386APSARA CLINICAL DIAG. & INFO. SYSJJE1983-02-0986
K813161FLO TEM II (BLOOD/FLUID WARMERLGZ1981-12-0929
K803249FLUID WARMERLGZ1981-05-21149

Recalls

openFDA lists no recalls under a recalling firm named Datachem, Inc..

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.

Frequently asked questions

How many FDA 510(k) clearances are listed under Datachem, Inc.?

FDA lists 5 510(k) clearances under the applicant name “Datachem, Inc.” (first 1981, latest 1990), across 3 product codes in 2 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 Datachem, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Datachem, Inc. is 86 days.

Which FDA product codes appear under Datachem, Inc.?

The most frequent FDA product codes under this applicant name are JJE (Analyzer, Chemistry (Photometric, Discrete), For Clinical Use, 2); LGZ (Warmer, Thermal, Infusion Fluid, 2); CEM (Electrode, Ion Specific, Potassium, 1).

Next steps

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.

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