WAMPOLE HS-CRP ELISA
K-Number: K011855 · 2002-01-08
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Device Summary
Frequently Asked Questions
What is the WAMPOLE HS-CRP ELISA?
WAMPOLE HS-CRP ELISA is a medical device that received FDA 510(k) clearance on 2002-01-08. The listed applicant is Carter-Wallace, Inc.. The 510(k) number is K011855.
When did WAMPOLE HS-CRP ELISA receive FDA 510(k) clearance?
WAMPOLE HS-CRP ELISA received FDA 510(k) clearance on 2002-01-08, under 510(k) number K011855.
Who is the listed applicant for WAMPOLE HS-CRP ELISA?
The FDA 510(k) record lists Carter-Wallace, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WAMPOLE HS-CRP ELISA?
The FDA product code for WAMPOLE HS-CRP ELISA is DCN.
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: DCN)
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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