Atlas FDA

NANOLAS ND:YAG OPHTHALMIC LASER

FDA 510(k) clearance K881459 · decided 1988-04-13

Clearance details

K-number
K881459
Device name
NANOLAS ND:YAG OPHTHALMIC LASER
Applicant
Biophysic Medical, Inc.
Decision
Substantially Equivalent
Date received
1988-04-06
Decision date
1988-04-13
Days to decision
7 days
Clearance type
Traditional
Product code
LOI
Device class
3
Medical specialty
Unknown
Advisory committee
Unknown
Location
Pleasant Hill, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.