PHOTOVOLT PVA 4M+2 ANALYZER
K-Number: K800453 · 1980-03-20
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Device Summary
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.
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