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FDA 510(k)

NEWMED ABP-LITE

K-Number: K955887 · 1996-09-05

ApplicantNewmed Corp.
Decision Date1996-09-05
Product CodeDXW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NEWMED ABP-LITE is the device name listed in this FDA 510(k) record. The listed applicant is Newmed Corp.. It received FDA 510(k) clearance on 1996-09-05 under 510(k) number K955887. The device is classified under product code DXW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEWMED ABP-LITE?

NEWMED ABP-LITE is a medical device that received FDA 510(k) clearance on 1996-09-05. The listed applicant is Newmed Corp.. The 510(k) number is K955887.

When did NEWMED ABP-LITE receive FDA 510(k) clearance?

NEWMED ABP-LITE received FDA 510(k) clearance on 1996-09-05, under 510(k) number K955887.

Who is the listed applicant for NEWMED ABP-LITE?

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

What is the FDA product code for NEWMED ABP-LITE?

The FDA product code for NEWMED ABP-LITE is DXW.

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 Newmed 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.

K935955DOSER

Related Devices (Code: DXW)

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.

K972020OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITORCas Medical Systems, Inc.K802830MILLAR MIKRO-TIP CATHETER PHONOTRANSMillar Instruments, Inc.K800222MODEL 412 ELECTROFLUIDIC MANOMETERMed-Tek Corp.K800179INFRASONDE AUTO/INFLATOR ELEC. VIBRATORSphygmetrics, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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