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)

PHOTOVOLT PVA 4M+2 ANALYZER

K-Number: K800453 · 1980-03-20

Decision Date1980-03-20
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHOTOVOLT PVA 4M+2 ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Photovolt Corp.. It received FDA 510(k) clearance on 1980-03-20 under 510(k) number K800453. The device is classified under product code JJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTOVOLT PVA 4M+2 ANALYZER?

PHOTOVOLT PVA 4M+2 ANALYZER is a medical device that received FDA 510(k) clearance on 1980-03-20. The listed applicant is Photovolt Corp.. The 510(k) number is K800453.

When did PHOTOVOLT PVA 4M+2 ANALYZER receive FDA 510(k) clearance?

PHOTOVOLT PVA 4M+2 ANALYZER received FDA 510(k) clearance on 1980-03-20, under 510(k) number K800453.

Who is the listed applicant for PHOTOVOLT PVA 4M+2 ANALYZER?

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

What is the FDA product code for PHOTOVOLT PVA 4M+2 ANALYZER?

The FDA product code for PHOTOVOLT PVA 4M+2 ANALYZER is JJC.

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 Photovolt 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: JJC)

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.

↑