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

ARTHROSCOPE

K Number: K931792 · Decision Jun 13, 1994
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
11
Applicant Total
14
Review Days
427

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ARTHROSCOPE
K Number
K931792
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4350
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intramed Laboratories, Inc.
Date Received
April 12, 1993
Decision Date
June 13, 1994
Product Code
HRH
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HRH Trephine, Manual, Ophthalmic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HRH), ordered by most recent decision date.

View all

Other Clearances by Intramed Laboratories, Inc.

K Number Device Name
K953258 TITANIUM HEMOSTATIC CLIP
K942457 GRAFT THROMBECTOMY INSTRUMENTS
K925283 VALVULOTOME
K934696 ANGIOSCOPE
K922114 ENDOSCOPIC RETRIEVAL BASKET
K914385 OPTICAL VALVULOTOME
K904465 FLEXIBLE ARTHROSCOPE
K903528 LAPAROSCOPE
K902444 CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP
K901010 FLEXIBLE CHOLEDOCHOSCOPE
Search all 14 clearances from Intramed Laboratories, Inc. →