Med Service, Inc.: FDA clearances and approvals

Med Service, Inc. has 9 FDA 510(k) clearances (first 1987, latest 1988), across 2 product codes in 1 review panel. Median 510(k) review time: 77 days.

510(k) clearances per year

YearClearancesMedian review days
20120—
20130—
20140—
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20190—
20200—
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20260—

Top product codes

Product codeDeviceSubmissions510(k) clearances
FNLBed, Ac-Powered Adjustable Hospital66
FNJBed, Manual33

Review panels

Most recent Med Service, Inc. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K881961MSI STANDARD BED MODELS: L1097-64 AND L1085-64FNJ1988-11-01175
K881960MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74FNL1988-11-01175
K881782MSI 4000 SERIES BEDFNL1988-07-1277
K881964MSI 3003 SERIES BEDFNJ1988-06-2849
K881963MSI 3002 SERIES BEDFNL1988-06-2849
K881962MSI 2005 SERIES BEDFNJ1988-06-0324
K881965MSI 5000 SERIES BEDFNL1988-05-3121
K881027MSI 2002 SERIES BEDFNL1988-05-2677
K873291MSI 9000 SERIES BEDFNL1987-12-30135

Recalls

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

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 Med Service, Inc. have?

Med Service, Inc. has 9 FDA 510(k) clearances (first 1987, latest 1988), across 2 product codes in 1 review panel.

How long does FDA take to clear Med Service, Inc.'s 510(k)s?

The median time from FDA receipt to decision across Med Service, Inc.'s cleared 510(k)s is 77 days.

What devices does Med Service, Inc. make?

Its most frequent FDA product codes are FNL (Bed, Ac-Powered Adjustable Hospital, 6); FNJ (Bed, Manual, 3).

Has Med Service, Inc. had device recalls?

openFDA lists no recalls under a recalling firm name matching Med Service, Inc. 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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