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FDA 510(k)

MONAGHAN'S PRESSURE ALARM

K-Number: K821649 · 1982-08-05

ApplicantMonaghan Medical Corp.
Decision Date1982-08-05
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONAGHAN'S PRESSURE ALARM is the device name listed in this FDA 510(k) record. The listed applicant is Monaghan Medical Corp.. It received FDA 510(k) clearance on 1982-08-05 under 510(k) number K821649. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONAGHAN'S PRESSURE ALARM?

MONAGHAN'S PRESSURE ALARM is a medical device that received FDA 510(k) clearance on 1982-08-05. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K821649.

When did MONAGHAN'S PRESSURE ALARM receive FDA 510(k) clearance?

MONAGHAN'S PRESSURE ALARM received FDA 510(k) clearance on 1982-08-05, under 510(k) number K821649.

Who is the listed applicant for MONAGHAN'S PRESSURE ALARM?

The FDA 510(k) record lists Monaghan Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONAGHAN'S PRESSURE ALARM?

The FDA product code for MONAGHAN'S PRESSURE ALARM 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.

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Other records listing Monaghan Medical 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.

K123945STRIVE DUAL ZONE PEAK FLOW METERK031514MODIFICATION TO TRUPEAK PEAK FLOW METERK023097TRUEZONE PEAK FLOW METERK012939AEROVENT II CHC COLLAPSIBLE HOLDING CHAMBERK991212MODIFICATION TO TRUZONE PEAK FLOW METERK964130AEROGEAR ASTHMA ACTION KIT

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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.

K201666SINGLE USE MANOMETERFlexicare Medical Limited.K182292VORTRAN APM-PlusVortran Medical Technology 1, Inc.K180510NS 120P-TRS Airway Pressure GaugeInstrumentation Industries, Inc.K172284NAPA LP-15 Airway Pressure MonitorDrw Medical, LLCK153733VORTRAN ManometerVortran Medical Technology 1, Inc.K122627GIO DIGITAL PRESSURE GUAGESGalemed Corp.

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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