FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PERCU GUIDE I (LOOP TYPE)

K Number: K863090 · Decision Aug 29, 1986
Classifications
1
FEI Numbers
236
Registration Numbers
236
Same Product Code
27
Applicant Total
56
Review Days
16

Basic Information

Device Name
PERCU GUIDE I (LOOP TYPE)
K Number
K863090
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
E-Z-EM, INC.
Date Received
August 13, 1986
Decision Date
August 29, 1986
Product Code
GDF
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GDF Guide, Needle, Surgical

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