CAMPYLOBACTER SUPPLEMENT-BLASER/WANG
K-Number: K850307 · 1985-03-20
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Device Summary
Frequently Asked Questions
What is the CAMPYLOBACTER SUPPLEMENT-BLASER/WANG?
CAMPYLOBACTER SUPPLEMENT-BLASER/WANG is a medical device that received FDA 510(k) clearance on 1985-03-20. The listed applicant is Pro-Lab, Inc.. The 510(k) number is K850307.
When did CAMPYLOBACTER SUPPLEMENT-BLASER/WANG receive FDA 510(k) clearance?
CAMPYLOBACTER SUPPLEMENT-BLASER/WANG received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850307.
Who is the listed applicant for CAMPYLOBACTER SUPPLEMENT-BLASER/WANG?
The FDA 510(k) record lists Pro-Lab, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAMPYLOBACTER SUPPLEMENT-BLASER/WANG?
The FDA product code for CAMPYLOBACTER SUPPLEMENT-BLASER/WANG is JSK.
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 Pro-Lab, Inc. 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: JSK)
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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