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

ENDOSCOPIC APPLICATOR

K Number: K120608 · Decision Mar 15, 2012
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
29
Review Days
15

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Basic Information

Device Name
ENDOSCOPIC APPLICATOR
K Number
K120608
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micromedics, Inc.
Date Received
February 29, 2012
Decision Date
March 15, 2012
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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Other Clearances by Micromedics, Inc.

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K102563 SINGLE CANNULA EXTENDED APPLICATOR
K100754 GRAFT DELIVERY SYSTEM MODEL SA-6115
K073401 EARPOPPER, MODEL EP-2000, EP-2100, EP-3000
K061092 BAXTER DUPLOSPRAY MIS APPLICATOR
K051157 INSTRU-SAFE INSTRUMENT PROTECTION SYSTEMS
K050340 MICROMEDICS SPHENOID SINUS STENT
K042834 MICROMEDICS FIBRIJET AIR ASSISTED ENDOSCOPIC APPLICATOR
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