FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LACERATION TRAY

K Number: K955658 · Decision Jan 25, 1996
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
21
Review Days
44

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Basic Information

Device Name
LACERATION TRAY
K Number
K955658
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Transidyne General Corp.
Date Received
December 12, 1995
Decision Date
January 25, 1996
Product Code
FRG
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FRG Wrap, Sterilization

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Other Clearances by Transidyne General Corp.

K Number Device Name
K961217 BODILY FLUID DISPOSAL KIT
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K950743 ORAL PROCEDURE PACK
K950449 SURGICAL BUR
K950403 SURGICAL SAW BLADES
K924811 I.V. START KIT
K924243 TRACHEOSTOMY CARE KIT
K922339 SUTURE REMOVAL KIT
K922041 PRIMARY SURGICAL DRESSING TRAY
K897133 MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT
Search all 21 clearances from Transidyne General Corp. →