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)

LIQUID CHROMATOGRAPHIC DETECTOR LC-95

K-Number: K840977 · 1984-04-19

Decision Date1984-04-19
Product CodeKZR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUID CHROMATOGRAPHIC DETECTOR LC-95 is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1984-04-19 under 510(k) number K840977. The device is classified under product code KZR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CHROMATOGRAPHIC DETECTOR LC-95?

LIQUID CHROMATOGRAPHIC DETECTOR LC-95 is a medical device that received FDA 510(k) clearance on 1984-04-19. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K840977.

When did LIQUID CHROMATOGRAPHIC DETECTOR LC-95 receive FDA 510(k) clearance?

LIQUID CHROMATOGRAPHIC DETECTOR LC-95 received FDA 510(k) clearance on 1984-04-19, under 510(k) number K840977.

Who is the listed applicant for LIQUID CHROMATOGRAPHIC DETECTOR LC-95?

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

What is the FDA product code for LIQUID CHROMATOGRAPHIC DETECTOR LC-95?

The FDA product code for LIQUID CHROMATOGRAPHIC DETECTOR LC-95 is KZR.

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 The Perkin-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.

View all 62 devices →

Related Devices (Code: KZR)

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.

↑