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FDA 510(k)

PARA TECH PLUS RETICS

K-Number: K993825 · 1999-11-30

ApplicantStreck Laboratories, Inc.
Decision Date1999-11-30
Product CodeJCN
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PARA TECH PLUS RETICS 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 1999-11-30 under 510(k) number K993825. The device is classified under product code JCN. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARA TECH PLUS RETICS?

PARA TECH PLUS RETICS is a medical device that received FDA 510(k) clearance on 1999-11-30. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K993825.

When did PARA TECH PLUS RETICS receive FDA 510(k) clearance?

PARA TECH PLUS RETICS received FDA 510(k) clearance on 1999-11-30, under 510(k) number K993825.

Who is the listed applicant for PARA TECH PLUS RETICS?

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 PARA TECH PLUS RETICS?

The FDA product code for PARA TECH PLUS RETICS is JCN.

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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 KITK021922MODIFICATION TO PARA 5XK020469CAL-CHEX CD PLUS

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Related Devices (Code: JCN)

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.

K942209LIQUICHEK HEMATOLOGY-16 CONTROL, LOW, NORMAL AND HIGHBio-RadK934497CBC-STK(TM) HEMATOLOGY CONTROL/MULTIPLER&D Systems, Inc.K911582STAK-CHEXStreck Laboratories, Inc.K902389TRI-COUNT 16Hematronix, Inc.K902391CELL-DYN 3000 CONTROLUnipath , Ltd.K901875PARA 12 PLUSStreck Laboratories, Inc.

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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