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THEMALATOR. MODELS T-4-S, T-8-S, ETC.

FDA 510(k) clearance K950350 · decided 1995-03-24

Clearance details

K-number
K950350
Device name
THEMALATOR. MODELS T-4-S, T-8-S, ETC.
Applicant
Whitehall/Div Columbus Mckennon Corp.
Decision
Substantially Equivalent
Date received
1995-01-30
Decision date
1995-03-24
Days to decision
53 days
Clearance type
Traditional
Product code
IRQ
Device class
1
Regulation number
890.5950
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
City Of Industry, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.