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FDA 510(k)

DIGITAL PANEL METER

K-Number: K781255 · 1978-09-20

ApplicantRae Medical Corp.
Decision Date1978-09-20
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL PANEL METER is the device name listed in this FDA 510(k) record. The listed applicant is Rae Medical Corp.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781255. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL PANEL METER?

DIGITAL PANEL METER is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Rae Medical Corp.. The 510(k) number is K781255.

When did DIGITAL PANEL METER receive FDA 510(k) clearance?

DIGITAL PANEL METER received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781255.

Who is the listed applicant for DIGITAL PANEL METER?

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

What is the FDA product code for DIGITAL PANEL METER?

The FDA product code for DIGITAL PANEL METER is DRT.

Related Clinical Trials

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Other records listing Rae Medical 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.

K830321VENTURE II MONITORING SYSTEMK781256CATHODE RAY TUBE MED. DISPLAY

Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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