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

VIDEO ENDOSCOPE, RIGID

K Number: K903339 · Decision Mar 6, 1991
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
336
Applicant Total
18
Review Days
224

Basic Information

Device Name
VIDEO ENDOSCOPE, RIGID
K Number
K903339
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
MEDICAL DYNAMICS, INC.
Date Received
July 25, 1990
Decision Date
March 6, 1991
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

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Other Clearances by MEDICAL DYNAMICS, INC.

K Number Device Name
K974542 TRUE VISION, TRUE VISION II
K921294 VIDEO ENDOSCOPE-RIGID MODIFICATION
K934682 SURGICAL VIDEO CAMERA AND ACCESSORIES
K930568 ADAIR/VERESS NEEDLE INTRODUCER SET
K915538 OVER THE WIRE STONE BASKET
K914315 OPTICAL CATHETER INTRODUCER SETS, MODIFICATION
K913986 CHOLANGIOGRAPHY/CHOLANGIOSCOPY/LIHOPAXY SYSTEM
K911296 OPTICAL CATHETER ARTHROSCOPE
K904609 XENON LIGHT SOURCE
K904113 OPERATIVE RECORDING CAMERA
Search all 18 clearances from MEDICAL DYNAMICS, INC. →