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

STA-PUT NON-MAGNETIC INSTRUMENT DRAPE CATALOG #100-187-00 (16X20), 100-186-00 (16X10), 100-183-00 W/DEXTER WRAP

K Number: K950830 · Decision May 3, 1995
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
4
Review Days
68

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Basic Information

Device Name
STA-PUT NON-MAGNETIC INSTRUMENT DRAPE CATALOG #100-187-00 (16X20), 100-186-00 (16X10), 100-183-00 W/DEXTER WRAP
K Number
K950830
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Avail-Southwest Division
Date Received
February 24, 1995
Decision Date
May 3, 1995
Product Code
KKX
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
KKX Drape, Surgical, Antimicrobial

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Other Clearances by Avail-Southwest Division

K Number Device Name
K952678 STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT
K933520 ENDOSCOPIC ANTI-FOG KIT, 100-302-00
K864158 THERMAPAD