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FDA 510(k)

PRESSURE MANOMETER

K-Number: K110119 · 2011-06-10

ApplicantNeoforce Group, Inc.
Decision Date2011-06-10
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRESSURE MANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Neoforce Group, Inc.. It received FDA 510(k) clearance on 2011-06-10 under 510(k) number K110119. 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 PRESSURE MANOMETER?

PRESSURE MANOMETER is a medical device that received FDA 510(k) clearance on 2011-06-10. The listed applicant is Neoforce Group, Inc.. The 510(k) number is K110119.

When did PRESSURE MANOMETER receive FDA 510(k) clearance?

PRESSURE MANOMETER received FDA 510(k) clearance on 2011-06-10, under 510(k) number K110119.

Who is the listed applicant for PRESSURE MANOMETER?

The FDA 510(k) record lists Neoforce Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESSURE MANOMETER?

The FDA product code for PRESSURE MANOMETER is CAP.

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Other records listing Neoforce Group, 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.

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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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