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

PROPPER SHARPGUARD & TRAYPAD STERIL. AID

K Number: K802428 · Decision Oct 23, 1980
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
25
Review Days
17

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Basic Information

Device Name
PROPPER SHARPGUARD & TRAYPAD STERIL. AID
K Number
K802428
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Propper Mfg. Co., Inc.
Date Received
October 6, 1980
Decision Date
October 23, 1980
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 Propper Mfg. Co., Inc.

K Number Device Name
K111453 STEAM DOT BLU PROCESS INDICATOR
K102894 CLASSIX CHEMICAL STERILIZATION INDICATOR
K082620 ONCE-A-DAY VERTOS TEST PACK
K031152 PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)
K991618 BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATOR
K991276 PASS/FAIL CHALLENGE PACK
K973585 PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR
K972747 BI-O.K. EO GAS BIOLOGICAL TEST-PAK (269305,269310,269320)
K961156 ONCE-A-DAY BOWIE AND DICK TEST PACK.
K921798 PROPPER SUPER SERACULT(R)
Search all 25 clearances from Propper Mfg. Co., Inc. →