O-PERM 30
K-Number: K002703 · 2000-11-21
Advertisement
Device Summary
Frequently Asked Questions
What is the O-PERM 30?
O-PERM 30 is a medical device that received FDA 510(k) clearance on 2000-11-21. The listed applicant is Optical Polymer Research, Inc.. The 510(k) number is K002703.
When did O-PERM 30 receive FDA 510(k) clearance?
O-PERM 30 received FDA 510(k) clearance on 2000-11-21, under 510(k) number K002703.
Who is the listed applicant for O-PERM 30?
The FDA 510(k) record lists Optical Polymer Research, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for O-PERM 30?
The FDA product code for O-PERM 30 is HQD.
Other records listing Optical Polymer Research, 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: HQD)
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.
Advertisement