Atlas FDA

D.O.R.C. MICRODIATHERMY SYSTEM

FDA 510(k) clearance K962135 · decided 1996-08-29

Clearance details

K-number
K962135
Device name
D.O.R.C. MICRODIATHERMY SYSTEM
Applicant
Dutch Ophthalmic USA, Inc.
Decision
Substantially Equivalent
Date received
1996-06-03
Decision date
1996-08-29
Days to decision
87 days
Clearance type
Traditional
Product code
HQO
Device class
2
Regulation number
886.4115
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Kingston, NH, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.