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FDA 510(k)

YSI MODEL 23L LACTATE ANALYZER

K-Number: K822812 · 1982-12-13

ApplicantYellow Springs Instrument Co., Inc.
Decision Date1982-12-13
Product CodeHHP
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

YSI MODEL 23L LACTATE ANALYZER 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 1982-12-13 under 510(k) number K822812. The device is classified under product code HHP. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YSI MODEL 23L LACTATE ANALYZER?

YSI MODEL 23L LACTATE ANALYZER is a medical device that received FDA 510(k) clearance on 1982-12-13. The listed applicant is Yellow Springs Instrument Co., Inc.. The 510(k) number is K822812.

When did YSI MODEL 23L LACTATE ANALYZER receive FDA 510(k) clearance?

YSI MODEL 23L LACTATE ANALYZER received FDA 510(k) clearance on 1982-12-13, under 510(k) number K822812.

Who is the listed applicant for YSI MODEL 23L LACTATE ANALYZER?

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 MODEL 23L LACTATE ANALYZER?

The FDA product code for YSI MODEL 23L LACTATE ANALYZER is HHP.

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

K962070YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBEK922821YSI MODELS 4700 FOLEY CATHETER TEMPERATURE PROBESK922007YSI MODEL 441A AIRWAY TEMPERATURE PROBEK910633YSI MODEL 1500 BLOOD GLUCOSE ANALYZERK910718YSI PRECISION 4000 THERMOMETERK901131YSI MODEL 1500 SPORT L-LACTATE ANALYZER

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Related Devices (Code: HHP)

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.

K963505TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEMTenet Medical Engineering

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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