Contemporary Products, Inc.: FDA filings under this applicant name

FDA lists 5 510(k) clearances under the applicant name “Contemporary Products, Inc.” (first 1996, latest 2003), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 119 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
CAFNebulizer (Direct Patient Interface)22
NFBConserver, Oxygen22
JCXApparatus, Suction, Ward Use, Portable, Ac-Powered11

Review panels

Most recent Contemporary Products, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K0228656203NFB2003-02-13169
K992935OCD2001NFB2000-06-20294
K000543CONTEMPRO-MISTCAF2000-06-16119
K964994CPI MODEL 6240 50 PSI NEBULIZER COMPRESSORCAF1997-02-2167
K963558CPI MODEL 6260, 6260A OR 6261 OIL-LESS ASPIRATORJCX1996-12-0490

Recalls

openFDA lists no recalls under a recalling firm named Contemporary Products, 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.

Related HCPCS codes

HCPCS Level II codes whose descriptors match the device names of the product codes filed under Contemporary Products, Inc. (a text match, not an official crosswalk):

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

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

FDA lists 5 510(k) clearances under the applicant name “Contemporary Products, Inc.” (first 1996, latest 2003), 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 Contemporary Products, Inc.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Contemporary Products, Inc. is 119 days.

Which FDA product codes appear under Contemporary Products, Inc.?

The most frequent FDA product codes under this applicant name are CAF (Nebulizer (Direct Patient Interface), 2); NFB (Conserver, Oxygen, 2); JCX (Apparatus, Suction, Ward Use, Portable, Ac-Powered, 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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