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FDA 510(k)

YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP

K-Number: K823232 · 1982-12-07

ApplicantYellow Springs Instrument Co., Inc.
Decision Date1982-12-07
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP is the device name listed in this FDA 510(k) record. The listed applicant is Yellow Springs Instrument Co., Inc.. It received FDA 510(k) clearance on 1982-12-07 under 510(k) number K823232. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP?

YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP is a medical device that received FDA 510(k) clearance on 1982-12-07. The listed applicant is Yellow Springs Instrument Co., Inc.. The 510(k) number is K823232.

When did YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP receive FDA 510(k) clearance?

YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP received FDA 510(k) clearance on 1982-12-07, under 510(k) number K823232.

Who is the listed applicant for YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP?

The FDA 510(k) record lists Yellow Springs Instrument Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP?

The FDA product code for YSI #2650 SINGLE-DISPLAY OXYGEN & TEMP is CCL.

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Other records listing Yellow Springs Instrument Co., Inc. as applicant

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Related Devices (Code: CCL)

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.

K261389PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)Salter LabsK251245OxyMinder Pro (10310)Bio-Med Device, Inc.K250002Smart Check O2 (MA0236)Life Spark Medical, LLCK221734Maxtec MaxO2 ME+pMaxtec, LLCK213933Percent Oxygen SensorsCareox, LLCK213948OxyMinderBio-Med Devices, Inc.

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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