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

IMAGYN MICROLAP AND MICRO LAP-GOLD LAPAROSCOPES

K Number: K965055 · Decision Mar 6, 1997
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
19
Review Days
78

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Basic Information

Device Name
IMAGYN MICROLAP AND MICRO LAP-GOLD LAPAROSCOPES
K Number
K965055
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Imagyn Medical, Inc.
Date Received
December 18, 1996
Decision Date
March 6, 1997
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)

Similar 510(k) Clearances

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

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Other Clearances by Imagyn Medical, Inc.

K Number Device Name
K972426 MICROSPAN GOLD HYSTEROSCOPE AND MICROSPAN HYSTEROSCOPE SHEATH
K970750 MICROSPAN INSEMINATION SYSTEM
K971255 IMAGYN EXPANDABLE LAPAROSCOPIC INTRODUCER
K963580 IMAGYN FALLOPOSCOPY SYSTEM
K961688 MICROSPAN HYSTEROSCOPE
K961506 MICROSPAN HYSTEROSCOPE SHEATH
K952032 IMAGYN HYSTEROSCOPE SHEATHS
K951996 IMAGYN ENDOSCOPE
K951974 IMAGYN ENDOSCOPE SHEATH
K953201 IMAGYN UROSCOPE
Search all 19 clearances from Imagyn Medical, Inc. →