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

CUATICO MYELOGRAPHY NEEDLES

K Number: K813367 · Decision Jan 5, 1982
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
56
Review Days
36

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Basic Information

Device Name
CUATICO MYELOGRAPHY NEEDLES
K Number
K813367
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dlp, Inc.
Date Received
November 30, 1981
Decision Date
January 5, 1982
Product Code
GAA
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
GAA Needle, Aspiration And Injection, Disposable

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