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FDA 510(k)

TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST.

K-Number: K915637 · 1992-02-11

Decision Date1992-02-11
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST. is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Medical Technology, Inc.. It received FDA 510(k) clearance on 1992-02-11 under 510(k) number K915637. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST.?

TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST. is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Progressive Medical Technology, Inc.. The 510(k) number is K915637.

When did TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST. receive FDA 510(k) clearance?

TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST. received FDA 510(k) clearance on 1992-02-11, under 510(k) number K915637.

Who is the listed applicant for TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST.?

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

What is the FDA product code for TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST.?

The FDA product code for TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST. is IRP.

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 Progressive Medical Technology, 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.

Related Devices (Code: IRP)

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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