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FDA 510(k)

DBEST OCCULT BLOOD TEST KIT

K-Number: K984269 · 1999-05-11

ApplicantAmeritek, Inc.
Decision Date1999-05-11
Product CodeKHE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

DBEST OCCULT BLOOD 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 1999-05-11 under 510(k) number K984269. The device is classified under product code KHE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DBEST OCCULT BLOOD TEST KIT?

DBEST OCCULT BLOOD TEST KIT is a medical device that received FDA 510(k) clearance on 1999-05-11. The listed applicant is Ameritek, Inc.. The 510(k) number is K984269.

When did DBEST OCCULT BLOOD TEST KIT receive FDA 510(k) clearance?

DBEST OCCULT BLOOD TEST KIT received FDA 510(k) clearance on 1999-05-11, under 510(k) number K984269.

Who is the listed applicant for DBEST OCCULT BLOOD 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 OCCULT BLOOD TEST KIT?

The FDA product code for DBEST OCCULT BLOOD TEST KIT is KHE.

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Related Devices (Code: KHE)

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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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