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

VIDEO ENDOSCOPE-RIGID MODIFICATION

K Number: K921294 · Decision Jul 20, 1994
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
18
Review Days
855

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Basic Information

Device Name
VIDEO ENDOSCOPE-RIGID MODIFICATION
K Number
K921294
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medical Dynamics, Inc.
Date Received
March 17, 1992
Decision Date
July 20, 1994
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 Medical Dynamics, Inc.

K Number Device Name
K974542 TRUE VISION, TRUE VISION II
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
K903339 VIDEO ENDOSCOPE, RIGID
K904609 XENON LIGHT SOURCE
K904113 OPERATIVE RECORDING CAMERA
Search all 18 clearances from Medical Dynamics, Inc. →