ETEST ERTAPENEM
K-Number: K020748 · 2002-04-29
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Device Summary
Frequently Asked Questions
What is the ETEST ERTAPENEM?
ETEST ERTAPENEM is a medical device that received FDA 510(k) clearance on 2002-04-29. The listed applicant is Ab Biodisk. The 510(k) number is K020748.
When did ETEST ERTAPENEM receive FDA 510(k) clearance?
ETEST ERTAPENEM received FDA 510(k) clearance on 2002-04-29, under 510(k) number K020748.
Who is the listed applicant for ETEST ERTAPENEM?
The FDA 510(k) record lists Ab Biodisk as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ETEST ERTAPENEM?
The FDA product code for ETEST ERTAPENEM is JWY.
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 Ab Biodisk 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: JWY)
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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