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FDA 510(k)

FreezeSpray TA

K-Number: K261684 · 2026-09-05

Decision Date2026-09-05
Product CodeMLY
DecisionSubstantially Equivalent

Device Summary

FreezeSpray TA is the device name listed in this FDA 510(k) record. The listed applicant is Cryosurgery, Inc.. It received FDA 510(k) clearance on 2026-09-05 under 510(k) number K261684. The device is classified under product code MLY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FreezeSpray TA?

FreezeSpray TA is a medical device that received FDA 510(k) clearance on 2026-09-05. The listed applicant is Cryosurgery, Inc.. The 510(k) number is K261684.

When did FreezeSpray TA receive FDA 510(k) clearance?

FreezeSpray TA received FDA 510(k) clearance on 2026-09-05, under 510(k) number K261684.

Who is the listed applicant for FreezeSpray TA?

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

What is the FDA product code for FreezeSpray TA?

The FDA product code for FreezeSpray TA is MLY.

Other records listing Cryosurgery, 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.

Related Devices (Code: MLY)

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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