RESPI-PAK RT-PAK
K-Number: K910452 · 1991-04-16
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Device Summary
Frequently Asked Questions
What is the RESPI-PAK RT-PAK?
RESPI-PAK RT-PAK is a medical device that received FDA 510(k) clearance on 1991-04-16. The listed applicant is Cns, Inc.. The 510(k) number is K910452.
When did RESPI-PAK RT-PAK receive FDA 510(k) clearance?
RESPI-PAK RT-PAK received FDA 510(k) clearance on 1991-04-16, under 510(k) number K910452.
Who is the listed applicant for RESPI-PAK RT-PAK?
The FDA 510(k) record lists Cns, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESPI-PAK RT-PAK?
The FDA product code for RESPI-PAK RT-PAK is BZG.
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 Cns, Inc. 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: BZG)
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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