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FDA 510(k)

PHOTOTHERAPY/PROCEDURE LAMP

K-Number: K771025 · 1977-10-25

Decision Date1977-10-25
Product CodeLBI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHOTOTHERAPY/PROCEDURE LAMP is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771025. The device is classified under product code LBI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTOTHERAPY/PROCEDURE LAMP?

PHOTOTHERAPY/PROCEDURE LAMP is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Cavitron Corp.. The 510(k) number is K771025.

When did PHOTOTHERAPY/PROCEDURE LAMP receive FDA 510(k) clearance?

PHOTOTHERAPY/PROCEDURE LAMP received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771025.

Who is the listed applicant for PHOTOTHERAPY/PROCEDURE LAMP?

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

What is the FDA product code for PHOTOTHERAPY/PROCEDURE LAMP?

The FDA product code for PHOTOTHERAPY/PROCEDURE LAMP is LBI.

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 Cavitron 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 32 devices →

Related Devices (Code: LBI)

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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