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FDA 510(k)

TRAVONEB MODEL # TONE 1

K-Number: K854747 · 1986-02-24

ApplicantTravomed, Inc.
Decision Date1986-02-24
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRAVONEB MODEL # TONE 1 is the device name listed in this FDA 510(k) record. The listed applicant is Travomed, Inc.. It received FDA 510(k) clearance on 1986-02-24 under 510(k) number K854747. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAVONEB MODEL # TONE 1?

TRAVONEB MODEL # TONE 1 is a medical device that received FDA 510(k) clearance on 1986-02-24. The listed applicant is Travomed, Inc.. The 510(k) number is K854747.

When did TRAVONEB MODEL # TONE 1 receive FDA 510(k) clearance?

TRAVONEB MODEL # TONE 1 received FDA 510(k) clearance on 1986-02-24, under 510(k) number K854747.

Who is the listed applicant for TRAVONEB MODEL # TONE 1?

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

What is the FDA product code for TRAVONEB MODEL # TONE 1?

The FDA product code for TRAVONEB MODEL # TONE 1 is BTI.

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 Travomed, 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.

K864127MECHANICAL OXYGEN REGULATORK854748TRAVELPAK MODEL DC-202K854509TRAVELPAK MODEL AC-102

Related Devices (Code: BTI)

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.

K131881OMBRA TABLE TOP COMPRESSORTrudell Medical Intl.K113338MEDICAL AIR COMPRESSOROricare, Inc.K091871DK50 DSEkom S.R.O.K072634EMG TRITON -COMP,MODEL NCA01-XXX SERIESEmg Technology Co., Ltd.K060781MEDICAL COMPRESSOR, MODELS DK50 D AND DMEkom S.R.O.K051691MINIMATE COMPRESSORPrecision Medical, 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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