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FDA 510(k)

MONITOR, CITADEL INTRAVASCULAR PO2

K-Number: K760350 · 1976-10-29

ApplicantSherwood Medical Industries
Decision Date1976-10-29
Product CodeCCE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONITOR, CITADEL INTRAVASCULAR PO2 is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-10-29 under 510(k) number K760350. 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 MONITOR, CITADEL INTRAVASCULAR PO2?

MONITOR, CITADEL INTRAVASCULAR PO2 is a medical device that received FDA 510(k) clearance on 1976-10-29. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760350.

When did MONITOR, CITADEL INTRAVASCULAR PO2 receive FDA 510(k) clearance?

MONITOR, CITADEL INTRAVASCULAR PO2 received FDA 510(k) clearance on 1976-10-29, under 510(k) number K760350.

Who is the listed applicant for MONITOR, CITADEL INTRAVASCULAR PO2?

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

What is the FDA product code for MONITOR, CITADEL INTRAVASCULAR PO2?

The FDA product code for MONITOR, CITADEL INTRAVASCULAR PO2 is CCE.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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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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