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CRYOcheck™ Abnormal 1 Reference Control ARP1-10

by Precision Biologic

CRYOcheck™ Abnormal 1 Reference Control ARP1-10 is a Class II device made by Precision Biologic, cleared under FDA 510(k) K952624 on 30 Oct 1995 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00843876000084), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K952624

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00843876000084 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK952624 Date30 Oct 1995DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K952624 decided 30 Oct 1995 Active
  • FDA GUDID UDI-DI 00843876000084 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K952624
  2. Listed FDA GUDID 00843876000084

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
CRYOcheck™ Abnormal 1 Reference Control
Generic name
Multiple coagulation marker IVD, control
Model / reference
ARP1-10
Primary DI / UDI-DI
00843876000084
510(k) Number
FDA product code
GGN, GGC
GMDN term
Multiple coagulation marker IVD, control
Device class
Class II
Regulation number
864.5425
GUDID distribution status
In Commercial Distribution

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Properties

  • Lot / batch number
  • Expiration date
Other properties (13, all answered No)