ClearanceBrief
Company ยท US

Merocel Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1995. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KMFBandage, Liquid3
EMXBalloon, Epistaxis2
LYASplint, Intranasal Septal2
BTRTube, Tracheal (W/Wo Connector)1
EFQGauze/Sponge, Internal1
KHJPolymer, Ent Synthetic-Polyamide (Mesh Or Foil Material)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 14, 1995K954919MEROCEL SOFT WOUND DRESSING
Merocel Corp.
KMF
Sep 12, 1995K953072MEROCEL VAGINAL PACK
Merocel Corp.
EFQ
Aug 29, 1995K953013MEROCEL REINFORCED SILICONE SHEETS
Merocel Corp.
KHJ
Sep 16, 1994K943718EPISTAT-II NASAL CATHETER
Merocel Corp.
EMX
Jun 7, 1994K940572MEROCEL(R) WOUND DRESSING (WITH HEMOSTATIC CLAIM)
Merocel Corp.
KMF
Mar 4, 1994K935658MEROCEL(R) TURBINATE GLOVE AND SEPTAL SPLINT
Merocel Corp.
LYA
Aug 17, 1993K933152MEROCEL MEROSPLINT
Merocel Corp.
LYA
Aug 6, 1993K931565MEROCEL WOUND DRESSING
Merocel Corp.
KMF
Mar 18, 1993K920394MEROCEL EPISTACIS KIT
Merocel Corp.
EMX
Apr 6, 1992K910463MEROCEL(R) LASER-GUARD(TM)
Merocel Corp.
BTR

Latest recalls

DateFirm and productCodeLinked 510(k)
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