Atlas FDA

PARALLEL BARS

FDA 510(k) clearance K770611 · decided 1977-04-08

Clearance details

K-number
K770611
Device name
PARALLEL BARS
Applicant
Will Ross Co.
Decision
Substantially Equivalent
Date received
1977-03-31
Decision date
1977-04-08
Days to decision
8 days
Clearance type
Traditional
Product code
IOE
Device class
1
Regulation number
890.5370
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
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
BARS, PARALLEL, EXERCISE (K830466)Kaye Products, Inc.1983-03-09

Recalls involving this device

No recalls on record reference this clearance.