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FDA 510(k)

REAGENT KIT, LANCER GLUCOSE

K-Number: K790197 · 1979-03-12

ApplicantSherwood Medical Industries
Decision Date1979-03-12
Product CodeJJF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

REAGENT KIT, LANCER GLUCOSE 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 1979-03-12 under 510(k) number K790197. The device is classified under product code JJF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENT KIT, LANCER GLUCOSE?

REAGENT KIT, LANCER GLUCOSE is a medical device that received FDA 510(k) clearance on 1979-03-12. The listed applicant is Sherwood Medical Industries. The 510(k) number is K790197.

When did REAGENT KIT, LANCER GLUCOSE receive FDA 510(k) clearance?

REAGENT KIT, LANCER GLUCOSE received FDA 510(k) clearance on 1979-03-12, under 510(k) number K790197.

Who is the listed applicant for REAGENT KIT, LANCER GLUCOSE?

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 REAGENT KIT, LANCER GLUCOSE?

The FDA product code for REAGENT KIT, LANCER GLUCOSE is JJF.

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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: JJF)

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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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