Atlas FDA

THERMO-K

FDA 510(k) clearance K820814 · decided 1982-04-29

Clearance details

K-number
K820814
Device name
THERMO-K
Applicant
American Medical Systems, Inc.
Decision
Substantially Equivalent
Date received
1982-03-24
Decision date
1982-04-29
Days to decision
36 days
Clearance type
Traditional
Product code
DWJ
Device class
2
Regulation number
870.5900
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS (P940012/S002)American Medical Systems, Inc.1998-12-23
600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS (P940012/S001)American Medical Systems, Inc.1998-01-09
600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS (P940012)American Medical Systems, Inc.1995-12-27