Atlas FDA

CARBON FIBER COUCH INSERT

FDA 510(k) clearance K950068 · decided 1995-04-06

Clearance details

K-number
K950068
Device name
CARBON FIBER COUCH INSERT
Applicant
Medtec, Inc.
Decision
Substantially Equivalent
Date received
1995-01-09
Decision date
1995-04-06
Days to decision
87 days
Clearance type
Traditional
Product code
KXJ
Device class
2
Regulation number
892.1980
Medical specialty
Radiology
Advisory committee
Radiology
Location
Orange City, IA, US
Third-party review
No
Expedited review
No

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CAG-02A (K922098)Toshiba America Medical Systems, In.C1992-07-27
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RADKOR, RF-159 (K883885)Radkor, Inc.1988-10-19
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Recalls involving this device

No recalls on record reference this clearance.