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

FOCUS STERILE SYRINGES

K Number: K811167 · Decision May 21, 1981
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
2
Review Days
23

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Basic Information

Device Name
FOCUS STERILE SYRINGES
K Number
K811167
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Stanford Laboratories
Date Received
April 28, 1981
Decision Date
May 21, 1981
Product Code
FMF
Advisory Committee
General Hospital
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
FMF Syringe, Piston

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K Number Device Name
K802982 GAUZE, ABSORBABLE X-RAY DETECT. LAP SPG.