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FDA 510(k)

M-PACT CORNEAL LIGHT SHIELD

K-Number: K993883 · 1999-12-21

ApplicantM-Pact Corp.
Decision Date1999-12-21
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

M-PACT CORNEAL LIGHT SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is M-Pact Corp.. It received FDA 510(k) clearance on 1999-12-21 under 510(k) number K993883. The device is classified under product code HOZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M-PACT CORNEAL LIGHT SHIELD?

M-PACT CORNEAL LIGHT SHIELD is a medical device that received FDA 510(k) clearance on 1999-12-21. The listed applicant is M-Pact Corp.. The 510(k) number is K993883.

When did M-PACT CORNEAL LIGHT SHIELD receive FDA 510(k) clearance?

M-PACT CORNEAL LIGHT SHIELD received FDA 510(k) clearance on 1999-12-21, under 510(k) number K993883.

Who is the listed applicant for M-PACT CORNEAL LIGHT SHIELD?

The FDA 510(k) record lists M-Pact Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M-PACT CORNEAL LIGHT SHIELD?

The FDA product code for M-PACT CORNEAL LIGHT SHIELD is HOZ.

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Related Devices (Code: HOZ)

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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