Life Corp.: FDA clearances and approvals

Life Corp. has 5 FDA 510(k) clearances (first 1986, latest 1991), across 1 product code in 1 review panel. Median 510(k) review time: 119 days.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
BTLVentilator, Emergency, Powered (Resuscitator)55

Review panels

Most recent Life Corp. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K910699LIFE-02 (NON-REFILLABLE CYLINDER)BTL1991-06-18119
K910435LIFE OXYGENPAC 6/12 LPMBTL1991-06-17137
K910434LIFE OXYGENPAC FOR TRAINED MEDICAL PERSONNELBTL1991-06-17137
K910201LIFE O2BTL1991-02-0114
K855092LIFE CORP. OXYGEN PACBTL1986-01-2132

Recalls

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

Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.

Frequently asked questions

How many FDA 510(k) clearances does Life Corp. have?

Life Corp. has 5 FDA 510(k) clearances (first 1986, latest 1991), across 1 product code in 1 review panel.

How long does FDA take to clear Life Corp.'s 510(k)s?

The median time from FDA receipt to decision across Life Corp.'s cleared 510(k)s is 119 days.

What devices does Life Corp. make?

Its most frequent FDA product codes are BTL (Ventilator, Emergency, Powered (Resuscitator), 5).

Has Life Corp. had device recalls?

openFDA lists no recalls under a recalling firm name matching Life Corp. Related entities may recall under other names.

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.

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