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FDA 510(k)

ICE BATON

K-Number: K012746 · 2001-11-14

ApplicantBehive, Ltd.
Decision Date2001-11-14
Product CodeLKX
DecisionSubstantially Equivalent

Device Summary

ICE BATON is the device name listed in this FDA 510(k) record. The listed applicant is Behive, Ltd.. It received FDA 510(k) clearance on 2001-11-14 under 510(k) number K012746. The device is classified under product code LKX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ICE BATON?

ICE BATON is a medical device that received FDA 510(k) clearance on 2001-11-14. The listed applicant is Behive, Ltd.. The 510(k) number is K012746.

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

ICE BATON received FDA 510(k) clearance on 2001-11-14, under 510(k) number K012746.

Who is the listed applicant for ICE BATON?

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

What is the FDA product code for ICE BATON?

The FDA product code for ICE BATON is LKX.

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Related Devices (Code: LKX)

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.

K172358InstaliefPrivi Medical Pte, Ltd.K113660COLD PACK, PLASTIC APPLICATOR (MEDICAL GRADE)-NON-CHEMICALCryotherapy Products, Inc.K072414CRYOSTATLil Drug Store Products, Inc.K042564HEMOR-RITE CRYOTHERAPHYFama Holdings International CorpK981428ANU ICECryoptherapy Pain Relief Products, Inc.K973590HEMORRELIEF DEVICEA.Stein - Regulatory Affairs Consulting

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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