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

SURGIPEEL SELF-SEAL PACKAGING SYSTEM

K Number: K820302 · Decision Feb 24, 1982
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
19
Review Days
20

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Basic Information

Device Name
SURGIPEEL SELF-SEAL PACKAGING SYSTEM
K Number
K820302
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Surgicot, Inc.
Date Received
February 4, 1982
Decision Date
February 24, 1982
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 Surgicot, Inc.

K Number Device Name
K962605 PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE)
K931270 SURGICLEAN ENZYMATIC INSTRUMENT CLEANER
K863122 ASSERT BIOLOGICAL/CHEMICAL INDICATOR 12 MONTH EXP.
K855101 ASSERT TM BIOLOGICAL/CHEMICAL INDICATOR
K854631 ASSERT EO BIOLOGICAL TEST PACK
K854902 SURGICOT STEAM TEST PACK
K840541 NEURO SPONGE
K840471 EYE SPEAR
K840470 SURGISCRIBE MARKING PEN
K830739 PRO-GUARD
Search all 19 clearances from Surgicot, Inc. →