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FDA 510(k)

PM 1800 CONSERVING DEVICE

K-Number: K001412 · 2001-03-20

ApplicantPrecision Medical, Inc.
Decision Date2001-03-20
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PM 1800 CONSERVING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical, Inc.. It received FDA 510(k) clearance on 2001-03-20 under 510(k) number K001412. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PM 1800 CONSERVING DEVICE?

PM 1800 CONSERVING DEVICE is a medical device that received FDA 510(k) clearance on 2001-03-20. The listed applicant is Precision Medical, Inc.. The 510(k) number is K001412.

When did PM 1800 CONSERVING DEVICE receive FDA 510(k) clearance?

PM 1800 CONSERVING DEVICE received FDA 510(k) clearance on 2001-03-20, under 510(k) number K001412.

Who is the listed applicant for PM 1800 CONSERVING DEVICE?

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

What is the FDA product code for PM 1800 CONSERVING DEVICE?

The FDA product code for PM 1800 CONSERVING DEVICE is NFB.

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Other records listing Precision Medical, 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.

K173807Accu O2 Oxygen AnalyzerK103563PRECISION PORTABLE OXYGEN CONCENTRATION MODEL 4150K103324PRECISION LIQUID OXYGEN SYSTEMK090781HELIO2 BLENDERK072348PRECISION OXYGEN CONCENTRATORK063096PRECISION OXYGEN MONITOR

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Related Devices (Code: NFB)

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.

K250322Respond OC Conserving Regulator (130-0800)Responsive RespiratoryK220591ProximaDynasthetics, LLCK221014Effortless Oxygen Conserver System Models Effortless Pro and Effortless MobileEffortless Oxygen, LLCK200401ApogeeIncoba Ltd D/B/A DynarisK151506Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen CannulaSalter LabsK131023THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMENMedical Products, LLC

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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