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

PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES

K Number: K905462 · Decision Feb 6, 1991
Classifications
1
FEI Numbers
285
Registration Numbers
286
Same Product Code
21
Applicant Total
14
Review Days
63

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Basic Information

Device Name
PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES
K Number
K905462
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Angiosystems, Inc.
Date Received
December 5, 1990
Decision Date
February 6, 1991
Product Code
LRP
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
LRP Tray, Surgical

Similar 510(k) Clearances

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Other Clearances by Angiosystems, Inc.

K Number Device Name
K905464 MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING
K905459 SURGICAL PROCEDURE TRAY/LAPAROSCOPY CHOLECYSTECTOM
K905461 PROCEDURE KIT/ROUTINE DENTAL PROCEDURES
K905466 STERILE DISPOSABLE SURGICAL DRAPE/ABDOMINAL DRAPE
K905465 STERILE DISPOS SURGICAL DRAPE/C-SECTION DRAPE
K905460 STERILE DISPOSABLE DRAPE/OPHTHALMIC SURGERY
K905463 GENERAL MEDICAL PROCEDURE KIT/SKIN PREPARATION
K864688 ARNOLD-KING PRESSURE DRESSING
K843258 ANGIO SYS BRACHIAL ANGIO DRAPE
K843259 ANGIO SYS FLUOROSCOPE DRAPE
Search all 14 clearances from Angiosystems, Inc. →