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FDA 510(k)

SEQUENTIAL CUFF INFLATION DEVICE

K-Number: K781358 · 1978-09-20

Decision Date1978-09-20
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SEQUENTIAL CUFF INFLATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781358. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEQUENTIAL CUFF INFLATION DEVICE?

SEQUENTIAL CUFF INFLATION DEVICE is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Medasonics, Inc.. The 510(k) number is K781358.

When did SEQUENTIAL CUFF INFLATION DEVICE receive FDA 510(k) clearance?

SEQUENTIAL CUFF INFLATION DEVICE received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781358.

Who is the listed applicant for SEQUENTIAL CUFF INFLATION DEVICE?

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 SEQUENTIAL CUFF INFLATION DEVICE?

The FDA product code for SEQUENTIAL CUFF INFLATION DEVICE is JOW.

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 Medasonics, Inc. 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.

View all 19 devices →

Related Devices (Code: JOW)

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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