MODIFICATION PURITAN-BENNETT INFANT PM2
K-Number: K922004 · 1992-05-28
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Device Summary
Frequently Asked Questions
What is the MODIFICATION PURITAN-BENNETT INFANT PM2?
MODIFICATION PURITAN-BENNETT INFANT PM2 is a medical device that received FDA 510(k) clearance on 1992-05-28. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K922004.
When did MODIFICATION PURITAN-BENNETT INFANT PM2 receive FDA 510(k) clearance?
MODIFICATION PURITAN-BENNETT INFANT PM2 received FDA 510(k) clearance on 1992-05-28, under 510(k) number K922004.
Who is the listed applicant for MODIFICATION PURITAN-BENNETT INFANT PM2?
The FDA 510(k) record lists Puritan Bennett Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION PURITAN-BENNETT INFANT PM2?
The FDA product code for MODIFICATION PURITAN-BENNETT INFANT PM2 is BTM.
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 Puritan Bennett Corp. 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: BTM)
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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