Atlas FDA

HAND SCREW CLAMP

FDA 510(k) clearance K761118 · decided 1976-12-02

Clearance details

K-number
K761118
Device name
HAND SCREW CLAMP
Applicant
Fred Sammons, Inc.
Decision
Substantially Equivalent
Date received
1976-11-19
Decision date
1976-12-02
Days to decision
13 days
Clearance type
Traditional
Product code
IOD
Device class
1
Regulation number
890.5350
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
DELUXE TRACTION EXERCISE GLOVE BK5035 (K831544)Fred Sammons, Inc.1983-06-24
SURGICAL TUBING (K823648)Fred Sammons, Inc.1983-01-21
ANKLE WEIGHTS (K823822)Danek Medical, Inc.1983-01-14
SOLID WOOD CONE (K823600)Fred Sammons, Inc.1982-12-22
COLOR CODED WEIGHT CUFFS (K813632)Fred Sammons, Inc.1982-01-19
THERAPY BENCH (K812319)Kaye Products, Inc.1981-08-31
CANVAS WEDGE (K790587)Maddak, Inc.1979-04-03
SANDBAGS, VARIOUS WEIGHTS (K772414)Fred Sammons, Inc.1978-02-01
FLEXION MITTENS (K771030)Stat Medical Corp.1977-06-27
SHEET METAL CLAMP (K761119)Fred Sammons, Inc.1976-12-02

Recalls involving this device

No recalls on record reference this clearance.