S & W Model 29

FDA 510(k) K830875 · S & W Enterprises, Inc.

Substantially Equivalent

510(k) numberK830875

Submission

Device name
S & W Model 29
Applicant
S & W Enterprises, Inc.
Walker, MI, US
Received
March 18, 1983
Decision date
April 8, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JFB – Table, Physical Therapy, Multi Function
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5880
Specialty
Physical Medicine

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More from Ceragem International, Inc.

510(k)DeviceDecision
K864817S&W Model High-Low Mat Table, Various ModelsINQ · Traditional 01/05/1987SE
K841145Tilt Table 53INQ · Traditional 04/13/1984SE
K832768S & W SW52E W/Power Back LiftLGX · Traditional 09/20/1983SE
K830873S & W Model AsoKNC · Traditional 05/13/1983SE
K830874S & W Model SW 37INQ · Traditional 04/08/1983SE

Questions and answers

When was S & W Model 29 cleared by the FDA?

S & W Model 29 (K830875) received a 510(k) decision of Substantially Equivalent on April 8, 1983, 21 days after the submission was received.

What is the product code of K830875?

The FDA product code is JFB – Table, Physical Therapy, Multi Function, a Class II (moderate risk) device regulated under 21 CFR 890.5880.