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FDA 510(k)

ANAGO DISPOSABLE INSTANT COLD PACK

K-Number: K926590 · 1993-05-26

ApplicantAnago, Inc.
Decision Date1993-05-26
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ANAGO DISPOSABLE INSTANT COLD PACK is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1993-05-26 under 510(k) number K926590. The device is classified under product code IMD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANAGO DISPOSABLE INSTANT COLD PACK?

ANAGO DISPOSABLE INSTANT COLD PACK is a medical device that received FDA 510(k) clearance on 1993-05-26. The listed applicant is Anago, Inc.. The 510(k) number is K926590.

When did ANAGO DISPOSABLE INSTANT COLD PACK receive FDA 510(k) clearance?

ANAGO DISPOSABLE INSTANT COLD PACK received FDA 510(k) clearance on 1993-05-26, under 510(k) number K926590.

Who is the listed applicant for ANAGO DISPOSABLE INSTANT COLD PACK?

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

What is the FDA product code for ANAGO DISPOSABLE INSTANT COLD PACK?

The FDA product code for ANAGO DISPOSABLE INSTANT COLD PACK is IMD.

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 Anago, 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 44 devices →

Related Devices (Code: IMD)

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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