FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking & PMS 🇺🇸 United States

CARPENTIER-EDWARDS FLEX. ANNULOPLASTY

K Number: K792441 · Decision Mar 17, 1980
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
74
Applicant Total
12
Review Days
109

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Basic Information

Device Name
CARPENTIER-EDWARDS FLEX. ANNULOPLASTY
K Number
K792441
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent - Subject to Tracking & PMS
Applicant
Edwards Laboratories
Date Received
November 29, 1979
Decision Date
March 17, 1980
Product Code
KRH
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
KRH Ring, Annuloplasty

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Other Clearances by Edwards Laboratories

K Number Device Name
K801552 MOD. 9542 FLOW-THRU INJECT. TEMP. SENSOR
K800655 MODEL 100 SPECTRAVIEW
K792034 INTEGRAL DISPOSABLE HOLDER CARPENTIER
K790047 CARDIAC OUTPUT COMPUTER, MDEL 9520A
K790022 DISPOSABLE HOLDER FOR BIOPROSTHESIS
K781535 AC ADAPTER:MODELS 9525,9526,9527
K771663 PROBE & CATHETER
K771046 VENA CAVA UMBRELLA FILTER, MODEL 7321
K760151 APPLICATOR,ANGIOGRAPHY (7310MOBIN-UDDIN)
K760152 FILTER (7220&7221 MOBIN-UDDIN VENA CAVA)
Search all 12 clearances from Edwards Laboratories →