MERCURY AIRWAY PRESSURE MANOMETER
K-Number: K954486 · 1996-04-25
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Device Summary
Frequently Asked Questions
What is the MERCURY AIRWAY PRESSURE MANOMETER?
MERCURY AIRWAY PRESSURE MANOMETER is a medical device that received FDA 510(k) clearance on 1996-04-25. The listed applicant is Mercury Medical. The 510(k) number is K954486.
When did MERCURY AIRWAY PRESSURE MANOMETER receive FDA 510(k) clearance?
MERCURY AIRWAY PRESSURE MANOMETER received FDA 510(k) clearance on 1996-04-25, under 510(k) number K954486.
Who is the listed applicant for MERCURY AIRWAY PRESSURE MANOMETER?
The FDA 510(k) record lists Mercury Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MERCURY AIRWAY PRESSURE MANOMETER?
The FDA product code for MERCURY AIRWAY PRESSURE MANOMETER is CAP.
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 Mercury 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: CAP)
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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