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FDA 510(k)

UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100

K-Number: K872896 · 1988-02-12

ApplicantAmerican Bentley
Decision Date1988-02-12
Product CodeCCE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100 is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1988-02-12 under 510(k) number K872896. The device is classified under product code CCE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100?

UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100 is a medical device that received FDA 510(k) clearance on 1988-02-12. The listed applicant is American Bentley. The 510(k) number is K872896.

When did UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100 receive FDA 510(k) clearance?

UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100 received FDA 510(k) clearance on 1988-02-12, under 510(k) number K872896.

Who is the listed applicant for UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100?

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

What is the FDA product code for UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100?

The FDA product code for UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100 is CCE.

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Other records listing American Bentley 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.

K873923INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTERK870804CARDIOPLEGIA HEAT EXCHANGER MODEL NO. HE-100K872167CARDIOTOMY/MEDIASTINAL AUTO. RESERVOIR CATR-3500K872133OXYGENATOR MODEL NO. BENTLEY 5 PLUSK870911INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALYK870269ELECTROSURGICAL MENISCUS CUTTER (EMC) MOD. AMC-100

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Related Devices (Code: CCE)

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.

K935778VIA 1-01 INFUSION PUMP/BLOOD CHEMISTRY SYSTEMVia Medical Corp.K912145SYSTEM ATHENA-PRODUCT ENHANCEMENTS, ANESTHESIAS & W Medico TeknikK910453TOPS NEEDLE TIP PROBE & PVC TIP PROBEBaxter Healthcare CorpK905397PB3200 INTRA-ARTERIAL BLOOD GAS MONITORING SYSTEMPuritan Bennett Corp.K896311OPTEX BLOOD GAS MONITORING SYSTEMOptex BiomedicalK890624TISSUE OXYGEN MONITOR SYSTEM, MODEL IIBaxter Healthcare 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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