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

NOTCH-NEEDLE, WESCOTT STYLE

K Number: K870896 · Decision Mar 18, 1987
Classifications
1
FEI Numbers
321
Registration Numbers
322
Same Product Code
106
Applicant Total
9
Review Days
13

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Basic Information

Device Name
NOTCH-NEEDLE, WESCOTT STYLE
K Number
K870896
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ocean Medical Products, Ltd.
Date Received
March 5, 1987
Decision Date
March 18, 1987
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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K882013 SOFT TISSUE BIOPSY DEVICE
K843719 SINGLE WALL INTRODUCER NEEDLE
K823693 MYELOGRAPHY NEEDLE
K823692 SPINAL NEEDLE
K813462 MADAYAG TYPE NEEDLE
K813448 POTTS-COURNAND STYLE NEEDLE
K813460 CHIBA SKINNY NEEDLE
K813461 PERCUTANEOUS ENTRY NEEDLE, SELDINGER