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FDA 510(k)

POLYSTYRENE MICROTITER PLATE IMMUNOSORB

K-Number: K830653 · 1983-04-08

Decision Date1983-04-08
Product CodeDGO
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

POLYSTYRENE MICROTITER PLATE IMMUNOSORB is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Reagent Tech.. It received FDA 510(k) clearance on 1983-04-08 under 510(k) number K830653. The device is classified under product code DGO. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYSTYRENE MICROTITER PLATE IMMUNOSORB?

POLYSTYRENE MICROTITER PLATE IMMUNOSORB is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is Diagnostic Reagent Tech.. The 510(k) number is K830653.

When did POLYSTYRENE MICROTITER PLATE IMMUNOSORB receive FDA 510(k) clearance?

POLYSTYRENE MICROTITER PLATE IMMUNOSORB received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830653.

Who is the listed applicant for POLYSTYRENE MICROTITER PLATE IMMUNOSORB?

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

What is the FDA product code for POLYSTYRENE MICROTITER PLATE IMMUNOSORB?

The FDA product code for POLYSTYRENE MICROTITER PLATE IMMUNOSORB is DGO.

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 Diagnostic Reagent Tech. 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.

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Related Devices (Code: DGO)

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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