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FDA 510(k)

DETER. OF PHOSPHOHEXOSE ISOMERASE

K-Number: K770577 · 1977-06-17

Decision Date1977-06-17
Product CodeKLJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DETER. OF PHOSPHOHEXOSE ISOMERASE is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1977-06-17 under 510(k) number K770577. The device is classified under product code KLJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DETER. OF PHOSPHOHEXOSE ISOMERASE?

DETER. OF PHOSPHOHEXOSE ISOMERASE is a medical device that received FDA 510(k) clearance on 1977-06-17. The listed applicant is Sigma Chemical Co.. The 510(k) number is K770577.

When did DETER. OF PHOSPHOHEXOSE ISOMERASE receive FDA 510(k) clearance?

DETER. OF PHOSPHOHEXOSE ISOMERASE received FDA 510(k) clearance on 1977-06-17, under 510(k) number K770577.

Who is the listed applicant for DETER. OF PHOSPHOHEXOSE ISOMERASE?

The FDA 510(k) record lists Sigma Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DETER. OF PHOSPHOHEXOSE ISOMERASE?

The FDA product code for DETER. OF PHOSPHOHEXOSE ISOMERASE is KLJ.

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 Sigma Chemical Co. 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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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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