COMPLETE BRAND LUBRICATING AND REWETTING DROPS
K-Number: K983150 · 1998-11-25
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Device Summary
Frequently Asked Questions
What is the COMPLETE BRAND LUBRICATING AND REWETTING DROPS?
COMPLETE BRAND LUBRICATING AND REWETTING DROPS is a medical device that received FDA 510(k) clearance on 1998-11-25. The listed applicant is Allergan, Inc.. The 510(k) number is K983150.
When did COMPLETE BRAND LUBRICATING AND REWETTING DROPS receive FDA 510(k) clearance?
COMPLETE BRAND LUBRICATING AND REWETTING DROPS received FDA 510(k) clearance on 1998-11-25, under 510(k) number K983150.
Who is the listed applicant for COMPLETE BRAND LUBRICATING AND REWETTING DROPS?
The FDA 510(k) record lists Allergan, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPLETE BRAND LUBRICATING AND REWETTING DROPS?
The FDA product code for COMPLETE BRAND LUBRICATING AND REWETTING DROPS is LPN.
Related Clinical Trials
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.
Other records listing Allergan, 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.
Related Devices (Code: LPN)
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.
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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