Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DBEST HCG 2 IU/ML TEST KIT

K-Number: K001215 · 2000-06-22

Decision Date2000-06-22
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DBEST HCG 2 IU/ML TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ameritek, Inc.. It received FDA 510(k) clearance on 2000-06-22 under 510(k) number K001215. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 17 devices →

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.

↑