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FDA 510(k)

CARDIOPNEUMOGRAPH

K-Number: K781292 · 1978-09-20

ApplicantStreet Electronics Corp.
Decision Date1978-09-20
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CARDIOPNEUMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Street Electronics Corp.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781292. 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 CARDIOPNEUMOGRAPH?

CARDIOPNEUMOGRAPH is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Street Electronics Corp.. The 510(k) number is K781292.

When did CARDIOPNEUMOGRAPH receive FDA 510(k) clearance?

CARDIOPNEUMOGRAPH received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781292.

Who is the listed applicant for CARDIOPNEUMOGRAPH?

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

What is the FDA product code for CARDIOPNEUMOGRAPH?

The FDA product code for CARDIOPNEUMOGRAPH is DRT.

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.

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Other records listing Street Electronics 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.

K790217GENERATOR, MODEL VG-1

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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