POLYSTYRENE MICROTITER PLATE IMMUNOSORB
K-Number: K830653 · 1983-04-08
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Device Summary
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.
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
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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