Medical Device Manufacturer · US , Mystic , CT

Merocel Corp. - FDA 510(k) Cleared Devices

10 submissions · 8 cleared · Since 1992

Total

Cleared

Denied

Merocel Corp. has 8 FDA 510(k) cleared medical devices. Based in Mystic, US.

Historical record: 8 cleared submissions from 1992 to 1995. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Merocel Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Merocel Corp.

10 devices

1-10 of 10

Cleared Nov 14, 1995

MEROCEL SOFT WOUND DRESSING

K954919 · KMF

General & Plastic Surgery · 19d

Cleared Sep 12, 1995

MEROCEL VAGINAL PACK

K953072 · EFQ

General & Plastic Surgery · 74d

Cleared Aug 29, 1995

MEROCEL REINFORCED SILICONE SHEETS

K953013 · KHJ

Ear, Nose, Throat · 61d

Cleared Sep 16, 1994

EPISTAT-II NASAL CATHETER

K943718 · EMX

Ear, Nose, Throat · 46d

Cleared Jun 07, 1994

MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM)

K940572 · KMF

General & Plastic Surgery · 119d

Cleared Mar 04, 1994

MEROCEL(R) TURBINATE GLOVE AND SEPTAL SPLINT

K935658 · LYA

Ear, Nose, Throat · 100d

Cleared Aug 17, 1993

MEROCEL MEROSPLINT

K933152 · LYA

Ear, Nose, Throat · 49d

Cleared Aug 06, 1993

MEROCEL WOUND DRESSING

K931565 · KMF

General & Plastic Surgery · 129d

Cleared Mar 18, 1993

MEROCEL EPISTACIS KIT

K920394 · EMX

Ear, Nose, Throat · 413d

Cleared Apr 06, 1992

MEROCEL(R) LASER-GUARD(TM)

K910463 · BTR

Anesthesiology · 437d

Merocel Corp. - FDA 510(k) Cleared Devices

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