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

CARDIOMEMO

K Number: K803286 · Decision Mar 17, 1981
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
12
Applicant Total
32
Review Days
77

Basic Information

Device Name
CARDIOMEMO
K Number
K803286
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3640
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
INSTROMEDIX, INC.
Date Received
December 30, 1980
Decision Date
March 17, 1981
Product Code
KRE
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
KRE Analyzer, Pacemaker Generator Function, Indirect

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KRE), ordered by most recent decision date.

View all

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. →