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

ASPIRATION NEEDLE

K Number: K780784 · Decision Aug 14, 1978
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
20
Review Days
94

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Basic Information

Device Name
ASPIRATION NEEDLE
K Number
K780784
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ferris Mfg. Corp.
Date Received
May 12, 1978
Decision Date
August 14, 1978
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

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K991729 FERRIS POLYOSTOMY STERILE WOUND DRESSING
K990906 FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER
K984539 FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING
K982306 POLYTUBE
K932913 FERRIS POLYMEM HYDROPHILIC WOUND DRESSING
K900127 FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS)
K880330 FERRIS HYDROPHILIC DRESSING
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