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FDA 510(k)

MULTI-ENZYME LINEARITY SOLUTION

K-Number: K880266 · 1988-02-18

Decision Date1988-02-18
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTI-ENZYME LINEARITY SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Verichem Laboratories, Inc.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K880266. The device is classified under product code JJT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-ENZYME LINEARITY SOLUTION?

MULTI-ENZYME LINEARITY SOLUTION is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Verichem Laboratories, Inc.. The 510(k) number is K880266.

When did MULTI-ENZYME LINEARITY SOLUTION receive FDA 510(k) clearance?

MULTI-ENZYME LINEARITY SOLUTION received FDA 510(k) clearance on 1988-02-18, under 510(k) number K880266.

Who is the listed applicant for MULTI-ENZYME LINEARITY SOLUTION?

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

What is the FDA product code for MULTI-ENZYME LINEARITY SOLUTION?

The FDA product code for MULTI-ENZYME LINEARITY SOLUTION is JJT.

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 Verichem 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.

View all 14 devices →

Related Devices (Code: JJT)

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

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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