Medical Device Manufacturer · US , Lenexa , KS

Remel, L.P. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1996

Total

Cleared

Denied

Remel, L.P. has 10 FDA 510(k) cleared microbiology devices. Based in Lenexa, US.

Historical record: 10 cleared submissions from 1996 to 1997.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Remel, L.P. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Remel, L.P.

10 devices

1-10 of 10

Cleared Aug 28, 1997

REMEL BILE ESCULIN AZIDE AGAR W/6 MCG/ML VANCOMYCIN

K972359 · JSO

Microbiology · 64d

Cleared Feb 07, 1997

REMEL STAPH LATEX KIT

K964315 · JWX

Microbiology · 101d

Cleared Dec 06, 1996

REMEL MEROPENEM 10UG SUSCEPTIBILITY DISK

GENTAMICIN DISK (120MCG)

K961818 · JTN

Microbiology · 61d

Cleared Jul 10, 1996

STREPTOMYCIN DISK (300MCG)

K961819 · JTN

Microbiology · 61d

Cleared Mar 25, 1996

MUELLER HINTON AGAR WITH 2% NACI

Remel, L.P. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Remel, L.P.

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