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FDA 510(k)

PRO-GLASS

K-Number: K991844 · 1999-07-21

ApplicantCad Cam Ventures
Decision Date1999-07-21
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRO-GLASS is the device name listed in this FDA 510(k) record. The listed applicant is Cad Cam Ventures. It received FDA 510(k) clearance on 1999-07-21 under 510(k) number K991844. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-GLASS?

PRO-GLASS is a medical device that received FDA 510(k) clearance on 1999-07-21. The listed applicant is Cad Cam Ventures. The 510(k) number is K991844.

When did PRO-GLASS receive FDA 510(k) clearance?

PRO-GLASS received FDA 510(k) clearance on 1999-07-21, under 510(k) number K991844.

Who is the listed applicant for PRO-GLASS?

The FDA 510(k) record lists Cad Cam Ventures as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRO-GLASS?

The FDA product code for PRO-GLASS is EIH.

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Related Devices (Code: EIH)

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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