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FDA 510(k)

INSURE PRO TEST

K-Number: K992695 · 1999-10-18

ApplicantInbios Intl., Inc.
Decision Date1999-10-18
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

INSURE PRO TEST is the device name listed in this FDA 510(k) record. The listed applicant is Inbios Intl., Inc.. It received FDA 510(k) clearance on 1999-10-18 under 510(k) number K992695. 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 INSURE PRO TEST?

INSURE PRO TEST is a medical device that received FDA 510(k) clearance on 1999-10-18. The listed applicant is Inbios Intl., Inc.. The 510(k) number is K992695.

When did INSURE PRO TEST receive FDA 510(k) clearance?

INSURE PRO TEST received FDA 510(k) clearance on 1999-10-18, under 510(k) number K992695.

Who is the listed applicant for INSURE PRO TEST?

The FDA 510(k) record lists Inbios Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSURE PRO TEST?

The FDA product code for INSURE PRO TEST is JHI.

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Other records listing Inbios Intl., 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.

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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.

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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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