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

TRAY, IRRIGATION, STERILE, BASIC

K Number: K770799 · Decision Jun 22, 1977
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
11
Review Days
51

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Basic Information

Device Name
TRAY, IRRIGATION, STERILE, BASIC
K Number
K770799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Lukens Corp.
Date Received
May 2, 1977
Decision Date
June 22, 1977
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 Lukens Corp.

K Number Device Name
K880230 SIXALYZER
K800102 STANFORD STERILE LAP SPONGES
K792471 STANFORD STERILE LAP SPONGES
K791495 LUKENS BONE WAX (GAMMA RADIATION)
K770797 TRAY, CATHETERIZATION W/FOLEY, STERILE
K770795 SHAVE PREP SET
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. →