R3 Large Head Liners
K-Number: K211330 · 2022-01-19
Device Summary
Frequently Asked Questions
What is the R3 Large Head Liners?
R3 Large Head Liners is a medical device that received FDA 510(k) clearance on 2022-01-19. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K211330.
When did R3 Large Head Liners receive FDA 510(k) clearance?
R3 Large Head Liners received FDA 510(k) clearance on 2022-01-19, under 510(k) number K211330.
Who is the listed applicant for R3 Large Head Liners?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for R3 Large Head Liners?
The FDA product code for R3 Large Head Liners is LPH.
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 Smith & Nephew, 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: LPH)
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.