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FDA 510(k)

PLETHYSMOGRAPH, STRAIN GAUGE

K-Number: K782132 · 1979-02-26

ApplicantMedasonics, Inc.
Decision Date1979-02-26
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PLETHYSMOGRAPH, STRAIN GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1979-02-26 under 510(k) number K782132. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLETHYSMOGRAPH, STRAIN GAUGE?

PLETHYSMOGRAPH, STRAIN GAUGE is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Medasonics, Inc.. The 510(k) number is K782132.

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

PLETHYSMOGRAPH, STRAIN GAUGE received FDA 510(k) clearance on 1979-02-26, under 510(k) number K782132.

Who is the listed applicant for PLETHYSMOGRAPH, STRAIN GAUGE?

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

What is the FDA product code for PLETHYSMOGRAPH, STRAIN GAUGE?

The FDA product code for PLETHYSMOGRAPH, STRAIN GAUGE is JOM.

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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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