FDA 510(k)

HEIMLICH MICRO TRACH

K-Number: K895130 · 1989-11-07

Decision Date1989-11-07

Product CodeBTO

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

HEIMLICH MICRO TRACH is the device name listed in this FDA 510(k) record. The listed applicant is Ballard Medical Products. It received FDA 510(k) clearance on 1989-11-07 under 510(k) number K895130. The device is classified under product code BTO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEIMLICH MICRO TRACH?

HEIMLICH MICRO TRACH is a medical device that received FDA 510(k) clearance on 1989-11-07. The listed applicant is Ballard Medical Products. The 510(k) number is K895130.

When did HEIMLICH MICRO TRACH receive FDA 510(k) clearance?

HEIMLICH MICRO TRACH received FDA 510(k) clearance on 1989-11-07, under 510(k) number K895130.

Who is the listed applicant for HEIMLICH MICRO TRACH?

The FDA 510(k) record lists Ballard Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEIMLICH MICRO TRACH?

The FDA product code for HEIMLICH MICRO TRACH is BTO.

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Related Devices (Code: BTO)

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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.