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

SHORTWAVE DIATHERMY MODEL 802

K Number: K780755 · Decision May 12, 1978
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
44
Applicant Total
27
Review Days
4

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Basic Information

Device Name
SHORTWAVE DIATHERMY MODEL 802
K Number
K780755
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5290
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Birtcher Corp.
Date Received
May 8, 1978
Decision Date
May 12, 1978
Product Code
IMJ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IMJ Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

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