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

CATHETER, MULTIPLE LUMEN

K Number: K820446 · Decision Mar 11, 1982
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
2
Applicant Total
56
Review Days
21

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Basic Information

Device Name
CATHETER, MULTIPLE LUMEN
K Number
K820446
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dlp, Inc.
Date Received
February 18, 1982
Decision Date
March 11, 1982
Product Code
GBP
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
GBP Catheter, Multiple Lumen

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