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FDA 510(k)

NBP CUFF

K-Number: K092999 · 2009-11-24

ApplicantDraeger Medical AG & Co. KG
Decision Date2009-11-24
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NBP CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical AG & Co. KG. It received FDA 510(k) clearance on 2009-11-24 under 510(k) number K092999. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NBP CUFF?

NBP CUFF is a medical device that received FDA 510(k) clearance on 2009-11-24. The listed applicant is Draeger Medical AG & Co. KG. The 510(k) number is K092999.

When did NBP CUFF receive FDA 510(k) clearance?

NBP CUFF received FDA 510(k) clearance on 2009-11-24, under 510(k) number K092999.

Who is the listed applicant for NBP CUFF?

The FDA 510(k) record lists Draeger Medical AG & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NBP CUFF?

The FDA product code for NBP CUFF is DXQ.

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Related Devices (Code: DXQ)

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.

K254287Medline Reusable Blood Pressure CuffMedline Industries, LPK260747YP-710T Series NIBP Cuff;YP-840T Series Disposable CuffNihon Kohden CorporationK253089NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)Shenzhen Best Electronics Co., Ltd.K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)Unimed Medical Supplies, Inc.K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)Baxter Healthcare CorporationK250765AViTA Arm Type Blood Pressure Monitor CuffAvita Corporation

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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