FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

NEURO SPONGE

K Number: K840541 · Decision Apr 23, 1984
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
110
Applicant Total
19
Review Days
75

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Basic Information

Device Name
NEURO SPONGE
K Number
K840541
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4450
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Surgicot, Inc.
Date Received
February 8, 1984
Decision Date
April 23, 1984
Product Code
GDY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GDY Gauze/Sponge, Internal, X-Ray Detectable

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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
K840471 EYE SPEAR
K840470 SURGISCRIBE MARKING PEN
K830739 PRO-GUARD
K820302 SURGIPEEL SELF-SEAL PACKAGING SYSTEM
Search all 19 clearances from Surgicot, Inc. →