HERRICK ULTIMATE PUNCTUM PLUG
K-Number: K963501 · 1997-04-14
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Device Summary
Frequently Asked Questions
What is the HERRICK ULTIMATE PUNCTUM PLUG?
HERRICK ULTIMATE PUNCTUM PLUG is a medical device that received FDA 510(k) clearance on 1997-04-14. The listed applicant is Lacrimedics, Inc.. The 510(k) number is K963501.
When did HERRICK ULTIMATE PUNCTUM PLUG receive FDA 510(k) clearance?
HERRICK ULTIMATE PUNCTUM PLUG received FDA 510(k) clearance on 1997-04-14, under 510(k) number K963501.
Who is the listed applicant for HERRICK ULTIMATE PUNCTUM PLUG?
The FDA 510(k) record lists Lacrimedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HERRICK ULTIMATE PUNCTUM PLUG?
The FDA product code for HERRICK ULTIMATE PUNCTUM PLUG is LZU.
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 Lacrimedics, 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: LZU)
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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