Atlas FDA

INNOSCAN EXAMINATION LIGHT

FDA 510(k) clearance K827796 · decided 1982-08-24

Clearance details

K-number
K827796
Device name
INNOSCAN EXAMINATION LIGHT
Applicant
Innomed Corp.
Decision
Substantially Equivalent
Date received
1982-07-29
Decision date
1982-08-24
Days to decision
26 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Rye Brook, NY, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.