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

BODILY FLUID DISPOSAL KIT

K Number: K961217 · Decision Jul 25, 1996
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
606
Applicant Total
21
Review Days
119

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Basic Information

Device Name
BODILY FLUID DISPOSAL KIT
K Number
K961217
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Transidyne General Corp.
Date Received
March 28, 1996
Decision Date
July 25, 1996
Product Code
FXX
Advisory Committee
General, Plastic Surgery
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
FXX Mask, Surgical

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Other Clearances by Transidyne General Corp.

K Number Device Name
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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. →