DBEST HCG 2 IU/ML TEST KIT
K-Number: K001215 · 2000-06-22
Advertisement
Device Summary
Frequently Asked Questions
What is the DBEST HCG 2 IU/ML TEST KIT?
DBEST HCG 2 IU/ML TEST KIT is a medical device that received FDA 510(k) clearance on 2000-06-22. The listed applicant is Ameritek, Inc.. The 510(k) number is K001215.
When did DBEST HCG 2 IU/ML TEST KIT receive FDA 510(k) clearance?
DBEST HCG 2 IU/ML TEST KIT received FDA 510(k) clearance on 2000-06-22, under 510(k) number K001215.
Who is the listed applicant for DBEST HCG 2 IU/ML TEST KIT?
The FDA 510(k) record lists Ameritek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DBEST HCG 2 IU/ML TEST KIT?
The FDA product code for DBEST HCG 2 IU/ML TEST KIT is JHI.
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 Ameritek, 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: JHI)
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.
Advertisement