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FDA 510(k)

LIQUID ENZYME ID 90133

K-Number: K981561 · 1998-07-24

ApplicantAlcon Laboratories
Decision Date1998-07-24
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LIQUID ENZYME ID 90133 is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1998-07-24 under 510(k) number K981561. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID ENZYME ID 90133?

LIQUID ENZYME ID 90133 is a medical device that received FDA 510(k) clearance on 1998-07-24. The listed applicant is Alcon Laboratories. The 510(k) number is K981561.

When did LIQUID ENZYME ID 90133 receive FDA 510(k) clearance?

LIQUID ENZYME ID 90133 received FDA 510(k) clearance on 1998-07-24, under 510(k) number K981561.

Who is the listed applicant for LIQUID ENZYME ID 90133?

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

What is the FDA product code for LIQUID ENZYME ID 90133?

The FDA product code for LIQUID ENZYME ID 90133 is LPN.

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Other records listing Alcon Laboratories as applicant

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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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