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

SNAPPER

K Number: K913608 · Decision Nov 29, 1991
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
9
Review Days
107

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Basic Information

Device Name
SNAPPER
K Number
K913608
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Healthtek, Inc.
Date Received
August 14, 1991
Decision Date
November 29, 1991
Product Code
KPE
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
KPE Container, I.V.

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Other Clearances by Healthtek, Inc.

K Number Device Name
K923448 EMPTY SOLUTION TRANSFER CONTAINER W/ DETACH LEG
K913985 TRANSFER-AID(TM)
K881590 ADFUSE(TM)
K874495 ADCOMP 4000 HP SYSTEM
K873848 RETROBULBAR NEEDLE
K860610 ADCOMP
K860372 FAST FLOW XX (AQUEOUS SOLUTION FILTER)
K854008 STATLOCK