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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K827584
Device Name JAPANESE MADE MICROWAVE THERAPY EQUIPMENT
Applicant
Heiwa Electronic Industrial Co., Ltd.
1510 Shimotawara, Shijonawate
Osaka,  JP 575
Correspondent
Heiwa Electronic Industrial Co., Ltd.
1510 Shimotawara, Shijonawate
Osaka,  JP 575
Date Received06/14/1982
Decision Date 07/14/1982
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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