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

THUMPER

K Number: K914854 · Decision Jan 24, 1992
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
12
Review Days
88

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Basic Information

Device Name
THUMPER
K Number
K914854
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Block Medical, Inc.
Date Received
October 28, 1991
Decision Date
January 24, 1992
Product Code
FRN
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
FRN Pump, Infusion

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Other Clearances by Block Medical, Inc.

K Number Device Name
K944692 C-SERIES HOMEPUMP
K940117 MID-500
K934551 VERIFUSE AMBULATORY PUMP
K935236 FLOW CONTROLLING EXTENSION SET
K932740 HOMEPUMP NSF
K904663 AUTO SASH (TM)
K914924 CHEMO PRIMING PIN(TM)
K914855 MULTIPLE DOSE CONTROLLER
K910695 AUTO SASH (TM)
K902891 VERIFUSE AMBULATORY PUMP
Search all 12 clearances from Block Medical, Inc. →