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

MEDITHERM

K Number: K894152 · Decision Jun 11, 1990
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
88
Applicant Total
13
Review Days
362

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Basic Information

Device Name
MEDITHERM
K Number
K894152
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5300
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Medical Equipment Designs, Inc.
Date Received
June 14, 1989
Decision Date
June 11, 1990
Product Code
IMI
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
IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat

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Other Clearances by Medical Equipment Designs, Inc.

K Number Device Name
K911308 CARDIOTRACE-I TRANSTELEPHONIC ECG RECEIV CONSOLE
K895375 MULTISPIRO
K851277 MICROSPIRO-SDS
K840908 CHESTAC-25F SPIROMETER
K840929 FRC 85 SERIES SPIROMETER
K821081 CHART PROJECTOR
K821084 UNIVERSAL TRIAL FRAMEE
K821107 EXOPHTHALMOMETER
K821083 P.D. METER
K821082 TRIAL LENS SET
Search all 13 clearances from Medical Equipment Designs, Inc. →