Atlas FDA

FLUORESCENT SUN LAMP FIXTURE

FDA 510(k) clearance K802291 · decided 1980-10-31

Clearance details

K-number
K802291
Device name
FLUORESCENT SUN LAMP FIXTURE
Applicant
Strato-Ray Co.
Decision
Substantially Equivalent
Date received
1980-09-19
Decision date
1980-10-31
Days to decision
42 days
Clearance type
Traditional
Product code
HJE
Device class
2
Regulation number
878.4580
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VALTRAC(R) INTRODUCER FORCEP (K922348)American Cyanamid Co.1992-06-09
EXAMINER 10 (K781698)American Sterilizer Co.1978-11-03

Recalls involving this device

No recalls on record reference this clearance.