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FDA 510(k)

AMBU RMT VALVE

K-Number: K873579 · 1987-12-30

ApplicantAmbu, Inc.
Decision Date1987-12-30
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AMBU RMT VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Ambu, Inc.. It received FDA 510(k) clearance on 1987-12-30 under 510(k) number K873579. 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 AMBU RMT VALVE?

AMBU RMT VALVE is a medical device that received FDA 510(k) clearance on 1987-12-30. The listed applicant is Ambu, Inc.. The 510(k) number is K873579.

When did AMBU RMT VALVE receive FDA 510(k) clearance?

AMBU RMT VALVE received FDA 510(k) clearance on 1987-12-30, under 510(k) number K873579.

Who is the listed applicant for AMBU RMT VALVE?

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

What is the FDA product code for AMBU RMT VALVE?

The FDA product code for AMBU RMT VALVE is BWF.

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Other records listing Ambu, Inc. as applicant

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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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