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FDA 510(k)

BTL-899TT

K-Number: K252963 · 2026-06-12

ApplicantBTL Industries, Inc.
Decision Date2026-06-12
Product CodeIMJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BTL-899TT is the device name listed in this FDA 510(k) record. The listed applicant is BTL Industries, Inc.. It received FDA 510(k) clearance on 2026-06-12 under 510(k) number K252963. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BTL-899TT?

BTL-899TT is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is BTL Industries, Inc.. The 510(k) number is K252963.

When did BTL-899TT receive FDA 510(k) clearance?

BTL-899TT received FDA 510(k) clearance on 2026-06-12, under 510(k) number K252963.

Who is the listed applicant for BTL-899TT?

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

What is the FDA product code for BTL-899TT?

The FDA product code for BTL-899TT is IMJ.

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.

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Other records listing BTL Industries, 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.

K253750BTL-785NEHK252561BTL-754FFK250309BTL-199K243290BTL-785MJK241516BTL-398K241270BTL-754

View all 34 devices →

Related Devices (Code: IMJ)

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.

K250376ViVYViatherm Therapeutics, LLCK243112Curapuls 670Enraf-Nonius, B.V.K223620Reprieve by RegenesisTMRegenesis Biomedical, Inc.K182363BTL-703BTL Industries, Inc.K173300ViaTherm BOOSTViatherm Therapeutics, LLCK162240ProMedTek Model C1400 Shortwave Diathermy DevicePromedtek, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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