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FDA 510(k)

CHEM CHEX THEOPHYLLINE CONTROL

K-Number: K920223 · 1992-06-10

Decision Date1992-06-10
Product CodeLAW
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

CHEM CHEX THEOPHYLLINE CONTROL 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 1992-06-10 under 510(k) number K920223. The device is classified under product code LAW. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEM CHEX THEOPHYLLINE CONTROL?

CHEM CHEX THEOPHYLLINE CONTROL is a medical device that received FDA 510(k) clearance on 1992-06-10. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K920223.

When did CHEM CHEX THEOPHYLLINE CONTROL receive FDA 510(k) clearance?

CHEM CHEX THEOPHYLLINE CONTROL received FDA 510(k) clearance on 1992-06-10, under 510(k) number K920223.

Who is the listed applicant for CHEM CHEX THEOPHYLLINE CONTROL?

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 CHEM CHEX THEOPHYLLINE CONTROL?

The FDA product code for CHEM CHEX THEOPHYLLINE CONTROL is LAW.

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.

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.

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Related Devices (Code: LAW)

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.

Official Source

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

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