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FDA 510(k)

DIGAPHOT PHOTOTHERAPY METER MODEL PT 145

K-Number: K780162 · 1978-03-27

ApplicantCavitron Corp.
Decision Date1978-03-27
Product CodeFTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DIGAPHOT PHOTOTHERAPY METER MODEL PT 145 is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1978-03-27 under 510(k) number K780162. The device is classified under product code FTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGAPHOT PHOTOTHERAPY METER MODEL PT 145?

DIGAPHOT PHOTOTHERAPY METER MODEL PT 145 is a medical device that received FDA 510(k) clearance on 1978-03-27. The listed applicant is Cavitron Corp.. The 510(k) number is K780162.

When did DIGAPHOT PHOTOTHERAPY METER MODEL PT 145 receive FDA 510(k) clearance?

DIGAPHOT PHOTOTHERAPY METER MODEL PT 145 received FDA 510(k) clearance on 1978-03-27, under 510(k) number K780162.

Who is the listed applicant for DIGAPHOT PHOTOTHERAPY METER MODEL PT 145?

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 DIGAPHOT PHOTOTHERAPY METER MODEL PT 145?

The FDA product code for DIGAPHOT PHOTOTHERAPY METER MODEL PT 145 is FTA.

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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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

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Related Devices (Code: FTA)

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.

K112133OASYS SURGICAL LIGHT CONTROLLEROasys HealthcareK102791EASYSUITE SURGICAL LIGHT CONTROL (ESLC)Image Stream Medical, Inc.K081698MAINSTREAM OR SURGICAL LIGHT CONTROL (MSLC)Image Stream Medical, Inc.K053321LIGHT GUARD LIGHT HANDLE AND LIGHT HANDLE COVERXodus Medical, Inc.K051505SCB/STERIS OR-LIGHT INTERFACE BOXKARL STORZ Endoscopy-America, Inc.K023704KSEA SCB ACC CONTROLKARL STORZ Endoscopy-America, Inc.

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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