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FDA 510(k)

PULSETAKER

K-Number: K782131 · 1979-01-15

Decision Date1979-01-15
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PULSETAKER is the device name listed in this FDA 510(k) record. The listed applicant is Van, Cott, Bagley, Cornwall & Mccarth. It received FDA 510(k) clearance on 1979-01-15 under 510(k) number K782131. 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 PULSETAKER?

PULSETAKER is a medical device that received FDA 510(k) clearance on 1979-01-15. The listed applicant is Van, Cott, Bagley, Cornwall & Mccarth. The 510(k) number is K782131.

When did PULSETAKER receive FDA 510(k) clearance?

PULSETAKER received FDA 510(k) clearance on 1979-01-15, under 510(k) number K782131.

Who is the listed applicant for PULSETAKER?

The FDA 510(k) record lists Van, Cott, Bagley, Cornwall & Mccarth as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PULSETAKER?

The FDA product code for PULSETAKER 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.

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.

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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