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

ELECTRO-PLETHYSMOGRAPH

K Number: K780761 · Decision Jun 30, 1978
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
52
Applicant Total
15
Review Days
52

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Basic Information

Device Name
ELECTRO-PLETHYSMOGRAPH
K Number
K780761
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2780
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Biotecx Laboratories, Inc.
Date Received
May 9, 1978
Decision Date
June 30, 1978
Product Code
JOM
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
JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

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