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FDA 510(k)

VISINE FOR CONTACTS

K-Number: K991620 · 1999-09-24

ApplicantPfizer, Inc.
Decision Date1999-09-24
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISINE FOR CONTACTS is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer, Inc.. It received FDA 510(k) clearance on 1999-09-24 under 510(k) number K991620. 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 VISINE FOR CONTACTS?

VISINE FOR CONTACTS is a medical device that received FDA 510(k) clearance on 1999-09-24. The listed applicant is Pfizer, Inc.. The 510(k) number is K991620.

When did VISINE FOR CONTACTS receive FDA 510(k) clearance?

VISINE FOR CONTACTS received FDA 510(k) clearance on 1999-09-24, under 510(k) number K991620.

Who is the listed applicant for VISINE FOR CONTACTS?

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

What is the FDA product code for VISINE FOR CONTACTS?

The FDA product code for VISINE FOR CONTACTS is LPN.

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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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