SOURCERER
K-Number: K884091 · 1989-02-02
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Device Summary
Frequently Asked Questions
What is the SOURCERER?
SOURCERER is a medical device that received FDA 510(k) clearance on 1989-02-02. The listed applicant is John Caunt Scientific , Ltd.. The 510(k) number is K884091.
When did SOURCERER receive FDA 510(k) clearance?
SOURCERER received FDA 510(k) clearance on 1989-02-02, under 510(k) number K884091.
Who is the listed applicant for SOURCERER?
The FDA 510(k) record lists John Caunt Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOURCERER?
The FDA product code for SOURCERER is JJJ.
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: JJJ)
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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