Atlas FDA

STORZ PLASTIC SURGERY & EXAMINATION LOUNGE 7000

FDA 510(k) clearance K845023 · decided 1985-01-28

Clearance details

K-number
K845023
Device name
STORZ PLASTIC SURGERY & EXAMINATION LOUNGE 7000
Applicant
Storz Instrument Co.
Decision
Substantially Equivalent
Date received
1984-12-27
Decision date
1985-01-28
Days to decision
32 days
Clearance type
Traditional
Product code
LGX
Device class
1
Regulation number
878.4960
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
St. Louis, MO, US
Third-party review
No
Expedited review
No

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MULTIPLE, MODEL #17 (K820823)Midmark Corp.1982-04-21
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Recalls involving this device

No recalls on record reference this clearance.