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FDA 510(k)

TISSUE PULSATOR

K-Number: K780683 · 1978-05-03

ApplicantPulsator Corp.
Decision Date1978-05-03
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TISSUE PULSATOR is the device name listed in this FDA 510(k) record. The listed applicant is Pulsator Corp.. It received FDA 510(k) clearance on 1978-05-03 under 510(k) number K780683. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE PULSATOR?

TISSUE PULSATOR is a medical device that received FDA 510(k) clearance on 1978-05-03. The listed applicant is Pulsator Corp.. The 510(k) number is K780683.

When did TISSUE PULSATOR receive FDA 510(k) clearance?

TISSUE PULSATOR received FDA 510(k) clearance on 1978-05-03, under 510(k) number K780683.

Who is the listed applicant for TISSUE PULSATOR?

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

What is the FDA product code for TISSUE PULSATOR?

The FDA product code for TISSUE PULSATOR is ISA.

Related Clinical Trials

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Related Devices (Code: ISA)

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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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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