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FDA 510(k)

INTERMITTENT COMPRESSION BOOT FOR OTC

K-Number: K991921 · 1999-08-13

ApplicantEischoco, Inc.
Decision Date1999-08-13
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTERMITTENT COMPRESSION BOOT FOR OTC is the device name listed in this FDA 510(k) record. The listed applicant is Eischoco, Inc.. It received FDA 510(k) clearance on 1999-08-13 under 510(k) number K991921. 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 INTERMITTENT COMPRESSION BOOT FOR OTC?

INTERMITTENT COMPRESSION BOOT FOR OTC is a medical device that received FDA 510(k) clearance on 1999-08-13. The listed applicant is Eischoco, Inc.. The 510(k) number is K991921.

When did INTERMITTENT COMPRESSION BOOT FOR OTC receive FDA 510(k) clearance?

INTERMITTENT COMPRESSION BOOT FOR OTC received FDA 510(k) clearance on 1999-08-13, under 510(k) number K991921.

Who is the listed applicant for INTERMITTENT COMPRESSION BOOT FOR OTC?

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

What is the FDA product code for INTERMITTENT COMPRESSION BOOT FOR OTC?

The FDA product code for INTERMITTENT COMPRESSION BOOT FOR OTC 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.

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Other records listing Eischoco, 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.

K964957INTERMITTENT COMPRESSOR SYSTEM

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.

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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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