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

RECEPTAL ATS TRAUMA KGA1900L

K Number: K772196 · Decision Dec 22, 1977
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
194
Applicant Total
69
Review Days
24

Basic Information

Device Name
RECEPTAL ATS TRAUMA KGA1900L
K Number
K772196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5830
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
SORENSEN RESEARCH
Date Received
November 28, 1977
Decision Date
December 22, 1977
Product Code
CAC
Advisory Committee
Anesthesiology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
CAC Apparatus, Autotransfusion

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K831939 TALL FLOOR STAND TFS-01
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