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FDA 510(k)

BRONCHOSCOPE SUCTION UNIT

K-Number: K841399 · 1984-07-18

ApplicantKeymed, Inc.
Decision Date1984-07-18
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BRONCHOSCOPE SUCTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1984-07-18 under 510(k) number K841399. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRONCHOSCOPE SUCTION UNIT?

BRONCHOSCOPE SUCTION UNIT is a medical device that received FDA 510(k) clearance on 1984-07-18. The listed applicant is Keymed, Inc.. The 510(k) number is K841399.

When did BRONCHOSCOPE SUCTION UNIT receive FDA 510(k) clearance?

BRONCHOSCOPE SUCTION UNIT received FDA 510(k) clearance on 1984-07-18, under 510(k) number K841399.

Who is the listed applicant for BRONCHOSCOPE SUCTION UNIT?

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

What is the FDA product code for BRONCHOSCOPE SUCTION UNIT?

The FDA product code for BRONCHOSCOPE SUCTION UNIT is BTA.

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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.

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