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FDA 510(k)

BOUGIE, FILIFORM, JACKSON

K-Number: K770959 · 1977-06-14

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1977-06-14
Product CodeKBI
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BOUGIE, FILIFORM, JACKSON is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1977-06-14 under 510(k) number K770959. The device is classified under product code KBI. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOUGIE, FILIFORM, JACKSON?

BOUGIE, FILIFORM, JACKSON is a medical device that received FDA 510(k) clearance on 1977-06-14. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K770959.

When did BOUGIE, FILIFORM, JACKSON receive FDA 510(k) clearance?

BOUGIE, FILIFORM, JACKSON received FDA 510(k) clearance on 1977-06-14, under 510(k) number K770959.

Who is the listed applicant for BOUGIE, FILIFORM, JACKSON?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOUGIE, FILIFORM, JACKSON?

The FDA product code for BOUGIE, FILIFORM, JACKSON is KBI.

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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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