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FDA 510(k)

CURAD KID SIZE INSTANT COLD PACK

K-Number: K920252 · 1992-02-11

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

Device Summary

CURAD KID SIZE INSTANT COLD PACK is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1992-02-11 under 510(k) number K920252. 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 CURAD KID SIZE INSTANT COLD PACK?

CURAD KID SIZE INSTANT COLD PACK is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K920252.

When did CURAD KID SIZE INSTANT COLD PACK receive FDA 510(k) clearance?

CURAD KID SIZE INSTANT COLD PACK received FDA 510(k) clearance on 1992-02-11, under 510(k) number K920252.

Who is the listed applicant for CURAD KID SIZE INSTANT COLD PACK?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURAD KID SIZE INSTANT COLD PACK?

The FDA product code for CURAD KID SIZE 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 Kendall Healthcare Products Co. Div.Of Tyco Health 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 66 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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