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FDA 510(k)

TROCKI BODY VENTRILATOR

K-Number: K813326 · 1981-12-22

ApplicantL.T.D. 3 Co.
Decision Date1981-12-22
Product CodeBYT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TROCKI BODY VENTRILATOR is the device name listed in this FDA 510(k) record. The listed applicant is L.T.D. 3 Co.. It received FDA 510(k) clearance on 1981-12-22 under 510(k) number K813326. The device is classified under product code BYT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROCKI BODY VENTRILATOR?

TROCKI BODY VENTRILATOR is a medical device that received FDA 510(k) clearance on 1981-12-22. The listed applicant is L.T.D. 3 Co.. The 510(k) number is K813326.

When did TROCKI BODY VENTRILATOR receive FDA 510(k) clearance?

TROCKI BODY VENTRILATOR received FDA 510(k) clearance on 1981-12-22, under 510(k) number K813326.

Who is the listed applicant for TROCKI BODY VENTRILATOR?

The FDA 510(k) record lists L.T.D. 3 Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TROCKI BODY VENTRILATOR?

The FDA product code for TROCKI BODY VENTRILATOR is BYT.

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Related Devices (Code: BYT)

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.

K082657RTX RESPIRATORMedivent LimitedK072290PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUSDima Italia SrlK924341HAYEK OSCILLATOR(TM)Respironics, Inc.K910947NEV-10 NEGATIVE PRESSURE VENTILATORLifecare Services, Inc.K905530PURITAN-BENNETT COMPANION 500 LIQUID OXYGEN SYSTEMPuritan Bennett Corp.K902764EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARMJ. H. Emerson Co.

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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