Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DETECTOR, IR, MODEL GC-33

K-Number: K770639 · 1977-06-24

Decision Date1977-06-24
Product CodeKZQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DETECTOR, IR, MODEL GC-33 is the device name listed in this FDA 510(k) record. The listed applicant is Peokin-Elmer Corp.. It received FDA 510(k) clearance on 1977-06-24 under 510(k) number K770639. The device is classified under product code KZQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DETECTOR, IR, MODEL GC-33?

DETECTOR, IR, MODEL GC-33 is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Peokin-Elmer Corp.. The 510(k) number is K770639.

When did DETECTOR, IR, MODEL GC-33 receive FDA 510(k) clearance?

DETECTOR, IR, MODEL GC-33 received FDA 510(k) clearance on 1977-06-24, under 510(k) number K770639.

Who is the listed applicant for DETECTOR, IR, MODEL GC-33?

The FDA 510(k) record lists Peokin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DETECTOR, IR, MODEL GC-33?

The FDA product code for DETECTOR, IR, MODEL GC-33 is KZQ.

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 Peokin-Elmer Corp. 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.

Related Devices (Code: KZQ)

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.

↑