Respitrace Corp.: FDA filings under this applicant name

FDA lists 6 510(k) clearances under the applicant name “Respitrace Corp.” (first 1978, latest 1986), across 1 product code in 1 review panel. Median 510(k) review time under this name: 96 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
BZKSpirometer, Monitoring (W/Wo Alarm)66

Review panels

Most recent Respitrace Corp. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K854956RESPIGRAPHBZK1986-03-2099
K852692RESPITRACE 300SCBZK1985-07-1519
K823780RESPITRACE 300SCBZK1984-01-20401
K823783RESPICOMBBZK1984-01-11392
K823782RESPITRACE SYSTEMBZK1983-03-0782
K772016RESPITRACEBZK1978-01-2693

Recalls

openFDA lists no recalls under a recalling firm named Respitrace Corp..

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 Respitrace Corp.?

FDA lists 6 510(k) clearances under the applicant name “Respitrace Corp.” (first 1978, latest 1986), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Respitrace Corp.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Respitrace Corp. is 96 days.

Which FDA product codes appear under Respitrace Corp.?

The most frequent FDA product codes under this applicant name are BZK (Spirometer, Monitoring (W/Wo Alarm), 6).

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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