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

LAPAROSCOPE

K Number: K903528 · Decision Sep 4, 1990
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
14
Review Days
29

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Basic Information

Device Name
LAPAROSCOPE
K Number
K903528
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Intramed Laboratories, Inc.
Date Received
August 6, 1990
Decision Date
September 4, 1990
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

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Other Clearances by Intramed Laboratories, Inc.

K Number Device Name
K953258 TITANIUM HEMOSTATIC CLIP
K942457 GRAFT THROMBECTOMY INSTRUMENTS
K931792 ARTHROSCOPE
K925283 VALVULOTOME
K934696 ANGIOSCOPE
K922114 ENDOSCOPIC RETRIEVAL BASKET
K914385 OPTICAL VALVULOTOME
K904465 FLEXIBLE ARTHROSCOPE
K902444 CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP
K901010 FLEXIBLE CHOLEDOCHOSCOPE
Search all 14 clearances from Intramed Laboratories, Inc. →