Atlas FDA

DYNAMETER 50 LB.

FDA 510(k) clearance K772415 · decided 1978-01-05

Clearance details

K-number
K772415
Device name
DYNAMETER 50 LB.
Applicant
Fred Sammons, Inc.
Decision
Substantially Equivalent
Date received
1977-12-27
Decision date
1978-01-05
Days to decision
9 days
Clearance type
Traditional
Product code
HRW
Device class
1
Regulation number
888.1250
Medical specialty
Orthopedic
Advisory committee
Orthopedic
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
JTECH COMMANDER AND ALGOMETER (K971407)J-Tech Medical, Inc.1998-04-20
DIGIT-GRIP WITH LCD (DGR002) (K970870)Nk Biotechnical Corp.1997-05-02
LIGHTSCOPE SET (K894557)Optik1989-08-07
HANDHELD DYNAMOMETER, MODEL #160 AND #111 (K861396)Spark Instruments & Academics, Inc.1986-05-02
PINCH GAUGE, 0-301 LBS. (K821631)Fred Sammons, Inc.1982-06-11
PINCH METER (K812343)Fred Sammons, Inc.1981-09-11
BK-7531 PAIN THRESHOLD/FINGER FORCE GAUG (K801719)Fred Sammons, Inc.1980-08-04
MUSCLE TESTING GUN (K791021)The Orthodyn Co.1979-06-15
PRESSURE MONITOR, MODEL 212 (K790302)Zatek1979-03-21
PINCH GUAGE (K772413)Fred Sammons, Inc.1978-01-05
JAMAR DYNAMOMETEO BK-7498 (K771288)Fred Sammons, Inc.1977-07-21

Recalls involving this device

No recalls on record reference this clearance.