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FDA 510(k)

ICE BAND

K-Number: K771002 · 1977-08-30

ApplicantNorcliff Thayer, Inc.
Decision Date1977-08-30
Product CodeIME
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ICE BAND is the device name listed in this FDA 510(k) record. The listed applicant is Norcliff Thayer, Inc.. It received FDA 510(k) clearance on 1977-08-30 under 510(k) number K771002. The device is classified under product code IME. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ICE BAND?

ICE BAND is a medical device that received FDA 510(k) clearance on 1977-08-30. The listed applicant is Norcliff Thayer, Inc.. The 510(k) number is K771002.

When did ICE BAND receive FDA 510(k) clearance?

ICE BAND received FDA 510(k) clearance on 1977-08-30, under 510(k) number K771002.

Who is the listed applicant for ICE BAND?

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

What is the FDA product code for ICE BAND?

The FDA product code for ICE BAND is IME.

Other records listing Norcliff Thayer, 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.

K890290BRACE (ORAFIX SPECIAL)K791576FORGET - DENTURE BONDING LIQUIDK780174ORABRITE

Related Devices (Code: IME)

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.

K923627COLD PACKFriendmed ProductsK915876HOTPADTen Comfort Corp.K921446HOT OR COLD PACK (THERMIPAQ)Thermionics Corp.K905207MICRO-AIRE SOFT-ICE, COLD THERAPY COMPRESSMicro Surgical Instruments Corp.K882413SUBOCCIPITAL ICE PILLOWFerguson MedicalK863654RE-HEATER, HOT PACKK & L Ent.

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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