OHMEDA MODULUS II PLUS ANESTHESIA SYSTEM
K-Number: K875350 · 1988-03-24
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Device Summary
Frequently Asked Questions
What is the OHMEDA MODULUS II PLUS ANESTHESIA SYSTEM?
OHMEDA MODULUS II PLUS ANESTHESIA SYSTEM is a medical device that received FDA 510(k) clearance on 1988-03-24. The listed applicant is Ohmeda Medical. The 510(k) number is K875350.
When did OHMEDA MODULUS II PLUS ANESTHESIA SYSTEM receive FDA 510(k) clearance?
OHMEDA MODULUS II PLUS ANESTHESIA SYSTEM received FDA 510(k) clearance on 1988-03-24, under 510(k) number K875350.
Who is the listed applicant for OHMEDA MODULUS II PLUS ANESTHESIA SYSTEM?
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 OHMEDA MODULUS II PLUS ANESTHESIA SYSTEM?
The FDA product code for OHMEDA MODULUS II PLUS ANESTHESIA SYSTEM 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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