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FDA 510(k)

HIPPURATE HYDROLYSIS TEST

K-Number: K861888 · 1986-06-03

ApplicantPro-Lab, Inc.
Decision Date1986-06-03
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HIPPURATE HYDROLYSIS TEST is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Lab, Inc.. It received FDA 510(k) clearance on 1986-06-03 under 510(k) number K861888. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIPPURATE HYDROLYSIS TEST?

HIPPURATE HYDROLYSIS TEST is a medical device that received FDA 510(k) clearance on 1986-06-03. The listed applicant is Pro-Lab, Inc.. The 510(k) number is K861888.

When did HIPPURATE HYDROLYSIS TEST receive FDA 510(k) clearance?

HIPPURATE HYDROLYSIS TEST received FDA 510(k) clearance on 1986-06-03, under 510(k) number K861888.

Who is the listed applicant for HIPPURATE HYDROLYSIS TEST?

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 HIPPURATE HYDROLYSIS TEST?

The FDA product code for HIPPURATE HYDROLYSIS TEST is JTO.

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Related Devices (Code: JTO)

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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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