AMBU RMT VALVE— 510(k) K873579

Substantially Equivalent

Ambu, Inc.

FDA 510(k) clearance K873579 for AMBU RMT VALVE, Substantially Equivalent on 1987-12-30. Applicant: Ambu, Inc.. Device class: 2.

Clearance details

Applicant: Ambu, Inc.
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1987-09-03
Decision date: 1987-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hanover, MD, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.