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FDA 510(k)

IN-LINE OXYGEN MONITORING SYSTEM

K-Number: K821159 · 1982-05-25

ApplicantG.D. Searle and Co.
Decision Date1982-05-25
Product CodeDRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IN-LINE OXYGEN MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1982-05-25 under 510(k) number K821159. The device is classified under product code DRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN-LINE OXYGEN MONITORING SYSTEM?

IN-LINE OXYGEN MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1982-05-25. The listed applicant is G.D. Searle and Co.. The 510(k) number is K821159.

When did IN-LINE OXYGEN MONITORING SYSTEM receive FDA 510(k) clearance?

IN-LINE OXYGEN MONITORING SYSTEM received FDA 510(k) clearance on 1982-05-25, under 510(k) number K821159.

Who is the listed applicant for IN-LINE OXYGEN MONITORING SYSTEM?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IN-LINE OXYGEN MONITORING SYSTEM?

The FDA product code for IN-LINE OXYGEN MONITORING SYSTEM is DRY.

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Other records listing G.D. Searle and Co. 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.

K811068BYPASS COILK811071VENOUS OXYGEN PROBEK803238INTRAVASCULAR CATHETERK810630SILICONE ELASTOMER COATED LATEX FOLEYK810131ADMINISTRATION SETK802485SEARLE VASCULAR LOOPS

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Related Devices (Code: DRY)

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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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