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

WECK TROCAR

K Number: K915378 · Decision Jun 29, 1992
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
140
Review Days
213

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Basic Information

Device Name
WECK TROCAR
K Number
K915378
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Edward Weck, Inc.
Date Received
November 29, 1991
Decision Date
June 29, 1992
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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K897045 BOWIE-DICK TEST CARD CATALOG NUMBER 008018
K871110 CORONARY ARTERY BYPASS GRAFT (CABG) MARKER
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