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

OWENS ENDOSCOPIC INSTRUMENTS AND ACCESSORIES

K Number: K926596 · Decision Jun 10, 1994
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
4
Review Days
639

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Basic Information

Device Name
OWENS ENDOSCOPIC INSTRUMENTS AND ACCESSORIES
K Number
K926596
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Owens Industries, Inc.
Date Received
September 9, 1992
Decision Date
June 10, 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 Owens Industries, Inc.

K Number Device Name
K926594 OWENS LAPAROSCOPY INSTRUMENTS AND ACCESSORIES
K926595 OWENS BIOPSY FORCEPS
K932796 OWENS TROCAR