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FDA 510(k)

RET-CHECK

K-Number: K900484 · 1990-03-09

ApplicantStreck Laboratories, Inc.
Decision Date1990-03-09
Product CodeGJR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RET-CHECK 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 1990-03-09 under 510(k) number K900484. The device is classified under product code GJR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RET-CHECK?

RET-CHECK is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K900484.

When did RET-CHECK receive FDA 510(k) clearance?

RET-CHECK received FDA 510(k) clearance on 1990-03-09, under 510(k) number K900484.

Who is the listed applicant for RET-CHECK?

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 RET-CHECK?

The FDA product code for RET-CHECK is GJR.

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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: GJR)

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.

K080016NRBC-CHEX FOR ADVIAStreckK060083NRBC-CHEX FOR LHStreckK000076CELL-CHEXStreck Laboratories, Inc.K940430SEDRATROLMedical Specialties Intl., 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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