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

DUAL HEAD STETHOSCOPE

K Number: K791338 · Decision Aug 10, 1979
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
153
Applicant Total
6
Review Days
21

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Basic Information

Device Name
DUAL HEAD STETHOSCOPE
K Number
K791338
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Amdia Medical Products
Date Received
July 20, 1979
Decision Date
August 10, 1979
Product Code
DQD
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
DQD Stethoscope, Electronic

Similar 510(k) Clearances

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

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Other Clearances by Amdia Medical Products

K Number Device Name
K791333 BOWLES STETHOSCOPE
K791335 NURSESCOPE
K791334 MULTISCOPE
K791337 TAYLOR NEUROLOGICAL HAMMER
K791336 BUCKS NEUROLOGICAL HAMMER