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Para Therm Bath

by Grimm Scientific Industries, Inc.

510(k) K842423

Para Therm Bath is a medical device (FDA Class II; FDA product code IMC, Bath, Paraffin) made by Grimm Scientific Industries, Inc., cleared under FDA 510(k) K842423 on 28 Jun 1984, active as of 10 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 10 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 10 Oct 2026.

Regulatory status

as of registry sync 10 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK842423 Date28 Jun 1984ClearedStatusActive

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  • Withdrawn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
IMC
Device class
Class II
Regulation
21 CFR Part 890.5110
Advisory committee
Physical Medicine
FDA decision
SESE Substantially Equivalent

Devices cleared under K842423

1 device · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K842423
UDI-DISize and differences
PARATherm
Grimm Scientific Industries, Inc.
PARATherm00861047000329 —On the market

Similar devices

Other devices filed under FDA product code IMC (Bath, Paraffin).

Other devices from Grimm Scientific Industries, Inc.

  • CRYOTherm

    Class II

  • PARATherm

    Class II

  • CRYOPress

    Class II

  • Cryotherm

    Class II

See all devices from Grimm Scientific Industries, Inc. →