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FDA 510(k)

INCENT-O-NEB

K-Number: K781731 · 1978-12-05

ApplicantB & F Medical Products, Inc.
Decision Date1978-12-05
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INCENT-O-NEB is the device name listed in this FDA 510(k) record. The listed applicant is B & F Medical Products, Inc.. It received FDA 510(k) clearance on 1978-12-05 under 510(k) number K781731. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INCENT-O-NEB?

INCENT-O-NEB is a medical device that received FDA 510(k) clearance on 1978-12-05. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K781731.

When did INCENT-O-NEB receive FDA 510(k) clearance?

INCENT-O-NEB received FDA 510(k) clearance on 1978-12-05, under 510(k) number K781731.

Who is the listed applicant for INCENT-O-NEB?

The FDA 510(k) record lists B & F Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INCENT-O-NEB?

The FDA product code for INCENT-O-NEB is BWF.

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Other records listing B & F Medical Products, Inc. as applicant

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Related Devices (Code: BWF)

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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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