Atlas FDA

STORZ #6500 POWER EXAMINATION CHAIR

FDA 510(k) clearance K820636 · decided 1982-03-26

Clearance details

K-number
K820636
Device name
STORZ #6500 POWER EXAMINATION CHAIR
Applicant
Storz Instrument Co.
Decision
Substantially Equivalent
Date received
1982-03-08
Decision date
1982-03-26
Days to decision
18 days
Clearance type
Traditional
Product code
GBB
Device class
1
Regulation number
878.4960
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
TENET TIBIAL FRACTURE SUPPORT (K964102)Tenet Medical Engineering1996-12-05
HYDRAULIC FOOT OPERATED STOOL (K893598)Arthro-Medic, Inc.1989-10-10
LITHOTOMY CHAIR #415 (K831385)Midmark Corp.1983-06-02
NUTROMAT (K831325)Medlog GmbH Marketing Services1983-06-02
NAGASHIMA SN OPERATOR'S CHAIR (K822264)Kelleher Corp.1982-10-13
EXAMINATION & TREATMENT CHAIRS (K822251)Kelleher Corp.1982-08-27
NAGASHIMA SN AUTOMATIC TREATMENT CHAIR (K822013)Kelleher Corp.1982-07-28

Recalls involving this device

No recalls on record reference this clearance.