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Para 4 215110

by Streck

Para 4 215110 is a Class II device made by Streck, cleared under FDA 510(k) K842017 on 26 Jun 1984 and listed in FDA GUDID since 14 Sep 2016 (UDI-DI 00844509000723), active as of 23 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 23 Oct 2026

Documents

510(k) K842017

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00844509000723 UDI-DI Date14 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK842017 Date26 Jun 1984DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K842017 decided 26 Jun 1984 Active
  • FDA GUDID UDI-DI 00844509000723 listed 14 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K842017
  2. Listed FDA GUDID 00844509000723

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Para 4
Generic name
Full blood count IVD, control
Model / Ref / Catalog
215110
Primary DI / UDI-DI
00844509000723
510(k) Number
FDA product code
JPK
GMDN term
Full blood count IVD, control
Device class
Class II
Regulation number
864.8625
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 1.5 Milliliter

Related devices

Category: Full blood count IVD, control

Cleared under the same submission (K842017)

and 8 more cleared under K842017

Similar devices in this category

Other devices filed under Full blood count IVD, control.

Other devices from Streck

See all devices from Streck →

Properties

  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)