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FDA 510(k)

STRAIN GAUGE PLETHYSMOGRAPH

K-Number: K781352 · 1978-10-27

ApplicantMedimatic
Decision Date1978-10-27
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STRAIN GAUGE PLETHYSMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Medimatic. It received FDA 510(k) clearance on 1978-10-27 under 510(k) number K781352. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRAIN GAUGE PLETHYSMOGRAPH?

STRAIN GAUGE PLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1978-10-27. The listed applicant is Medimatic. The 510(k) number is K781352.

When did STRAIN GAUGE PLETHYSMOGRAPH receive FDA 510(k) clearance?

STRAIN GAUGE PLETHYSMOGRAPH received FDA 510(k) clearance on 1978-10-27, under 510(k) number K781352.

Who is the listed applicant for STRAIN GAUGE PLETHYSMOGRAPH?

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

What is the FDA product code for STRAIN GAUGE PLETHYSMOGRAPH?

The FDA product code for STRAIN GAUGE PLETHYSMOGRAPH is DSB.

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 Medimatic 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: DSB)

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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