REVISED OHMEDA MODULUS II ANESTHESIA GAS MACHINE
K-Number: K890410 · 1989-04-12
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Device Summary
Frequently Asked Questions
What is the REVISED OHMEDA MODULUS II ANESTHESIA GAS MACHINE?
REVISED OHMEDA MODULUS II ANESTHESIA GAS MACHINE is a medical device that received FDA 510(k) clearance on 1989-04-12. The listed applicant is Ohmeda Medical. The 510(k) number is K890410.
When did REVISED OHMEDA MODULUS II ANESTHESIA GAS MACHINE receive FDA 510(k) clearance?
REVISED OHMEDA MODULUS II ANESTHESIA GAS MACHINE received FDA 510(k) clearance on 1989-04-12, under 510(k) number K890410.
Who is the listed applicant for REVISED OHMEDA MODULUS II ANESTHESIA GAS MACHINE?
The FDA 510(k) record lists Ohmeda Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REVISED OHMEDA MODULUS II ANESTHESIA GAS MACHINE?
The FDA product code for REVISED OHMEDA MODULUS II ANESTHESIA GAS MACHINE is BSZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Ohmeda Medical as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BSZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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