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Body Flex

by Conair Corp.

510(k) K942950

Body Flex is a medical device (FDA Class I; FDA product code ISA, Massager, Therapeutic, Electric) made by Conair Corp., cleared under FDA 510(k) K942950 on 26 Jul 1994, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SN Traditional NumberK942950 Date26 Jul 1994DecidedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
ISA
Device class
Class I
Regulation
21 CFR Part 890.5660
Advisory committee
Physical Medicine
FDA decision
SN

Similar devices

Other devices filed under FDA product code ISA (Massager, Therapeutic, Electric).

Other devices from Conair LLC.

See all devices from Conair LLC. →