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FDA 510(k)

MPR-4A - MICRO-PLATE READER

K-Number: K901965 · 1990-05-10

ApplicantTosoh Corp.
Decision Date1990-05-10
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MPR-4A - MICRO-PLATE READER is the device name listed in this FDA 510(k) record. The listed applicant is Tosoh Corp.. It received FDA 510(k) clearance on 1990-05-10 under 510(k) number K901965. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPR-4A - MICRO-PLATE READER?

MPR-4A - MICRO-PLATE READER is a medical device that received FDA 510(k) clearance on 1990-05-10. The listed applicant is Tosoh Corp.. The 510(k) number is K901965.

When did MPR-4A - MICRO-PLATE READER receive FDA 510(k) clearance?

MPR-4A - MICRO-PLATE READER received FDA 510(k) clearance on 1990-05-10, under 510(k) number K901965.

Who is the listed applicant for MPR-4A - MICRO-PLATE READER?

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

What is the FDA product code for MPR-4A - MICRO-PLATE READER?

The FDA product code for MPR-4A - MICRO-PLATE READER is JJQ.

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 Tosoh Corp. 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 11 devices →

Related Devices (Code: JJQ)

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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