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FDA 510(k)

MICROMEDIC REAGENT DISPENSER

K-Number: K803252 · 1981-01-12

Decision Date1981-01-12
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICROMEDIC REAGENT DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Micromedic Systems. It received FDA 510(k) clearance on 1981-01-12 under 510(k) number K803252. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROMEDIC REAGENT DISPENSER?

MICROMEDIC REAGENT DISPENSER is a medical device that received FDA 510(k) clearance on 1981-01-12. The listed applicant is Micromedic Systems. The 510(k) number is K803252.

When did MICROMEDIC REAGENT DISPENSER receive FDA 510(k) clearance?

MICROMEDIC REAGENT DISPENSER received FDA 510(k) clearance on 1981-01-12, under 510(k) number K803252.

Who is the listed applicant for MICROMEDIC REAGENT DISPENSER?

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

What is the FDA product code for MICROMEDIC REAGENT DISPENSER?

The FDA product code for MICROMEDIC REAGENT DISPENSER is JTC.

Related Clinical Trials

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.

Other records listing Micromedic Systems 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.

View all 42 devices →

Related Devices (Code: JTC)

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.

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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