REVISED PNEUMATIC DIAGRAMS FOR MODULUS II PLUS
K-Number: K882489 · 1988-07-08
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Device Summary
Frequently Asked Questions
What is the REVISED PNEUMATIC DIAGRAMS FOR MODULUS II PLUS?
REVISED PNEUMATIC DIAGRAMS FOR MODULUS II PLUS is a medical device that received FDA 510(k) clearance on 1988-07-08. The listed applicant is Ohmeda Medical. The 510(k) number is K882489.
When did REVISED PNEUMATIC DIAGRAMS FOR MODULUS II PLUS receive FDA 510(k) clearance?
REVISED PNEUMATIC DIAGRAMS FOR MODULUS II PLUS received FDA 510(k) clearance on 1988-07-08, under 510(k) number K882489.
Who is the listed applicant for REVISED PNEUMATIC DIAGRAMS FOR MODULUS II PLUS?
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 PNEUMATIC DIAGRAMS FOR MODULUS II PLUS?
The FDA product code for REVISED PNEUMATIC DIAGRAMS FOR MODULUS II PLUS 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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