COLLINS DIGITAL PULMONARY MANOMETER
K-Number: K912946 · 1992-01-15
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Device Summary
Frequently Asked Questions
What is the COLLINS DIGITAL PULMONARY MANOMETER?
COLLINS DIGITAL PULMONARY MANOMETER is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is Warren E. Collins, Inc.. The 510(k) number is K912946.
When did COLLINS DIGITAL PULMONARY MANOMETER receive FDA 510(k) clearance?
COLLINS DIGITAL PULMONARY MANOMETER received FDA 510(k) clearance on 1992-01-15, under 510(k) number K912946.
Who is the listed applicant for COLLINS DIGITAL PULMONARY MANOMETER?
The FDA 510(k) record lists Warren E. Collins, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLLINS DIGITAL PULMONARY MANOMETER?
The FDA product code for COLLINS DIGITAL PULMONARY MANOMETER is BXR.
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 Warren E. Collins, 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: BXR)
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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