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FDA 510(k)

ASTROSCAN 2100 MICROTITER PLATE READER

K-Number: K881458 · 1988-06-29

Decision Date1988-06-29
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ASTROSCAN 2100 MICROTITER PLATE READER is the device name listed in this FDA 510(k) record. The listed applicant is Astroscan , Ltd.. It received FDA 510(k) clearance on 1988-06-29 under 510(k) number K881458. 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 ASTROSCAN 2100 MICROTITER PLATE READER?

ASTROSCAN 2100 MICROTITER PLATE READER is a medical device that received FDA 510(k) clearance on 1988-06-29. The listed applicant is Astroscan , Ltd.. The 510(k) number is K881458.

When did ASTROSCAN 2100 MICROTITER PLATE READER receive FDA 510(k) clearance?

ASTROSCAN 2100 MICROTITER PLATE READER received FDA 510(k) clearance on 1988-06-29, under 510(k) number K881458.

Who is the listed applicant for ASTROSCAN 2100 MICROTITER PLATE READER?

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

What is the FDA product code for ASTROSCAN 2100 MICROTITER PLATE READER?

The FDA product code for ASTROSCAN 2100 MICROTITER 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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