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FDA 510(k)

QUADRA TITER MICRO PLATES

K-Number: K850725 · 1985-04-30

Decision Date1985-04-30
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

QUADRA TITER MICRO PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Microtech Medical Systems, Inc.. It received FDA 510(k) clearance on 1985-04-30 under 510(k) number K850725. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUADRA TITER MICRO PLATES?

QUADRA TITER MICRO PLATES is a medical device that received FDA 510(k) clearance on 1985-04-30. The listed applicant is Microtech Medical Systems, Inc.. The 510(k) number is K850725.

When did QUADRA TITER MICRO PLATES receive FDA 510(k) clearance?

QUADRA TITER MICRO PLATES received FDA 510(k) clearance on 1985-04-30, under 510(k) number K850725.

Who is the listed applicant for QUADRA TITER MICRO PLATES?

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

What is the FDA product code for QUADRA TITER MICRO PLATES?

The FDA product code for QUADRA TITER MICRO PLATES is LIB.

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 Microtech Medical Systems, 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.

View all 12 devices →

Related Devices (Code: LIB)

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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