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FDA 510(k)

TRAVELER NEBULIZING SYSTEM

K-Number: K832220 · 1983-09-26

ApplicantMedix of Florida, Inc.
Decision Date1983-09-26
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRAVELER NEBULIZING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medix of Florida, Inc.. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832220. 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 TRAVELER NEBULIZING SYSTEM?

TRAVELER NEBULIZING SYSTEM is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Medix of Florida, Inc.. The 510(k) number is K832220.

When did TRAVELER NEBULIZING SYSTEM receive FDA 510(k) clearance?

TRAVELER NEBULIZING SYSTEM received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832220.

Who is the listed applicant for TRAVELER NEBULIZING SYSTEM?

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

What is the FDA product code for TRAVELER NEBULIZING SYSTEM?

The FDA product code for TRAVELER NEBULIZING SYSTEM is BTI.

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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

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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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