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

RETROJECT(TM) ANTI-AIDS SYRINGE W/RETRAC. NEEDLE

K Number: K881980 · Decision Jun 28, 1988
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
5
Review Days
47

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Basic Information

Device Name
RETROJECT(TM) ANTI-AIDS SYRINGE W/RETRAC. NEEDLE
K Number
K881980
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Habley Medical Technology Corp.
Date Received
May 12, 1988
Decision Date
June 28, 1988
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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Other Clearances by Habley Medical Technology Corp.

K Number Device Name
K955164 S.A.R.S. II (SEMI-AUTOMATIC-RECONSTITUTING-SYSTEM)
K903007 MIRCAS DENTAL CARTRIDGE SYRINGE AND MIRCAS COVER
K880594 VACUGUARD(TM)
K871007 ANTI NEEDLE STRIKE ANTI DRUG ABUSE HYPO. SYRINGE