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

STANFORD STERILE LAP SPONGES

K Number: K800102 · Decision Jan 28, 1980
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
110
Applicant Total
11
Review Days
12

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Basic Information

Device Name
STANFORD STERILE LAP SPONGES
K Number
K800102
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4450
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Lukens Corp.
Date Received
January 16, 1980
Decision Date
January 28, 1980
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 Lukens Corp.

K Number Device Name
K880230 SIXALYZER
K792471 STANFORD STERILE LAP SPONGES
K791495 LUKENS BONE WAX (GAMMA RADIATION)
K770797 TRAY, CATHETERIZATION W/FOLEY, STERILE
K770795 SHAVE PREP SET
K770799 TRAY, IRRIGATION, STERILE, BASIC
K770796 SKIN SCRUB PREP SET
K770794 SUTURE REMOVAL SET, STERILE
K770798 BLADES, SURGICAL, STERILE
K770800 HANDLES, BLADE, SURGICAL
Search all 11 clearances from Lukens Corp. →