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Cryopress

by Grimm Scientific Industries, Inc.

510(k) K951769

Cryopress is a medical device (FDA Class II; FDA product code IRP, Massager, Powered Inflatable Tube) made by Grimm Scientific Industries, Inc., cleared under FDA 510(k) K951769 on 16 Oct 1995, 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)SESE Substantially Equivalent · Traditional NumberK951769 Date16 Oct 1995ClearedStatusActive

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  • Withdrawn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
IRP
Device class
Class II
Regulation
21 CFR Part 890.5650
Advisory committee
Physical Medicine
FDA decision
SESE Substantially Equivalent

Devices cleared under K951769

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 K951769
UDI-DISize and differences
CRYOPress
Grimm Scientific Industries, Inc.
CRYOPress00861047000312 —On the market

Similar devices

Other devices filed under FDA product code IRP (Massager, Powered Inflatable Tube).

Other devices from Grimm Scientific Industries, Inc.

  • CRYOTherm

    Class II

  • PARATherm

    Class II

  • CRYOPress

    Class II

  • Para Therm Bath

    Class II

See all devices from Grimm Scientific Industries, Inc. →