FDA 510(k)

SICKLE-CHEX

K-Number: K852107 · 1985-07-05

Decision Date1985-07-05

Product Code

DecisionSubstantially Equivalent

Device Summary

SICKLE-CHEX 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 1985-07-05 under 510(k) number K852107. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SICKLE-CHEX?

SICKLE-CHEX is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K852107.

When did SICKLE-CHEX receive FDA 510(k) clearance?

SICKLE-CHEX received FDA 510(k) clearance on 1985-07-05, under 510(k) number K852107.

Who is the listed applicant for SICKLE-CHEX?

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

Related Clinical Trials

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.

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Other records listing Streck Laboratories, Inc. as applicant

K042587RETIC-CHEX FOR CELL-DYN K040107CYTO-CHEX BCT K040025A1C-CELLULAR K023656SICKLE-CHEX SOLUBILITY KIT K021922MODIFICATION TO PARA 5X K020469CAL-CHEX CD PLUS

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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.