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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K837235
Device Name MODEL 920 ARGON LASER SYSTEM
Applicant
Coherent Radiation Laboratories
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Coherent Radiation Laboratories
4221 Richmond Rd., NW
Walker,  MI  49534
Date Received03/01/1983
Decision Date 04/04/1983
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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