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FDA 510(k)

MODIFICATION TO PARA 5X

K-Number: K021922 · 2002-06-25

ApplicantStreck Laboratories, Inc.
Decision Date2002-06-25
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO PARA 5X is the device name listed in this FDA 510(k) record. The listed applicant is Streck Laboratories, Inc.. It received FDA 510(k) clearance on 2002-06-25 under 510(k) number K021922. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO PARA 5X?

MODIFICATION TO PARA 5X is a medical device that received FDA 510(k) clearance on 2002-06-25. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K021922.

When did MODIFICATION TO PARA 5X receive FDA 510(k) clearance?

MODIFICATION TO PARA 5X received FDA 510(k) clearance on 2002-06-25, under 510(k) number K021922.

Who is the listed applicant for MODIFICATION TO PARA 5X?

The FDA 510(k) record lists Streck Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO PARA 5X?

The FDA product code for MODIFICATION TO PARA 5X is JPK.

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Other records listing Streck Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K042587RETIC-CHEX FOR CELL-DYNK040107CYTO-CHEX BCTK040025A1C-CELLULARK023656SICKLE-CHEX SOLUBILITY KITK020469CAL-CHEX CD PLUSK013316SICKLE-CHEX

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Related Devices (Code: JPK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K160586XN-L CHECKStreckK160590XN CHECKStreckK160588XN CHECK BFStreckK160606BC-5D Hematology ControlR&D Systems, Inc.K130962R&D 5D RETIC HEMATOLOGY CONTROLR&D Systems, Inc.K120744XN CHECK BFStreck

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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