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FDA 510(k)

NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS

K-Number: K081778 · 2008-09-12

ApplicantInstrumentation Industries, Inc.
Decision Date2008-09-12
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Industries, Inc.. It received FDA 510(k) clearance on 2008-09-12 under 510(k) number K081778. 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 NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS?

NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS is a medical device that received FDA 510(k) clearance on 2008-09-12. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K081778.

When did NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS receive FDA 510(k) clearance?

NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS received FDA 510(k) clearance on 2008-09-12, under 510(k) number K081778.

Who is the listed applicant for NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS?

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

What is the FDA product code for NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS?

The FDA product code for NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS is CAP.

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Other records listing Instrumentation Industries, 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.

K180510NS 120P-TRS Airway Pressure GaugeK162753RTC 26-C Inline Aerosol AdapterK113644PILOT TUBE REPAIR KITK102127ENDOTRACHEAL TUBE CHANGERSK101857RTC-24 VP METERED DOSE INHALER ADAPTER, MODEL RTC 24-VK091111RTC METERED DOSE INHALER ADAPTERS-SINGLE PATIENT USE, MODEL RTC 24-V, RTC MDI ADAPTER KIT-SINGLE PATIENT USE, MODEL RTC

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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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