PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES
K-Number: K915163 · 1992-01-06
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Device Summary
Frequently Asked Questions
What is the PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES?
PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES is a medical device that received FDA 510(k) clearance on 1992-01-06. The listed applicant is Biopool AB. The 510(k) number is K915163.
When did PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES receive FDA 510(k) clearance?
PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES received FDA 510(k) clearance on 1992-01-06, under 510(k) number K915163.
Who is the listed applicant for PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES?
The FDA 510(k) record lists Biopool AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES?
The FDA product code for PROTEIN S EID KIT AND PROTEIN S EID BULK PLATES is GGP.
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 Biopool AB 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: GGP)
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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