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

LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)

K Number: K925079 · Decision Aug 24, 1994
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
10
Review Days
686

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Basic Information

Device Name
LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)
K Number
K925079
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Endo Technic Corp.
Date Received
October 7, 1992
Decision Date
August 24, 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)

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Other Clearances by Endo Technic Corp.

K Number Device Name
K990908 MILLENNIUM
K971459 DERMALASE
K930756 LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECE
K925114 LAPAROSCOPIC INSTRUMENTS
K924058 TROCAR
K914825 1-125 ENDOSEED
K910200 LASER-35
K864976 SOLUSET CALCIUM DEMINERALIZING SOLUTION
K862129 SET CANAL SEALER PASTE