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

COMPRESSAR UNIVERSAL (TM) SYSTEM

K Number: K925809 · Decision Feb 22, 1993
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
32
Review Days
97

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Basic Information

Device Name
COMPRESSAR UNIVERSAL (TM) SYSTEM
K Number
K925809
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instromedix, Inc.
Date Received
November 17, 1992
Decision Date
February 22, 1993
Product Code
DXC
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXC Clamp, Vascular

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Other Clearances by Instromedix, Inc.

K Number Device Name
K964408 POSEIDON CARDIAC MONITORING SYSTEM (PCMS)
K964036 CARDIOMAGIC 2000 SOFTWARE
K955060 ACCELERATED TRANSMISSION PROTOCOL
K951096 LIFESIGNS RECEIVING CENER 2000 TRANSTELEPHONIC RECEIVER
K945476 HEARTHWATCH III(TM)
K950003 CARDIOMAGIC(R) SOFTWARE ENHANCEMENTS
K944362 HEARTCARD CARDIAC EVENT MONITOR
K943931 CARRYALL ENHANCEMENTS
K935586 PRINCE
K925639 CARDIOMAGIC SOFTWARE
Search all 32 clearances from Instromedix, Inc. →