dpl Faceware
K-Number: K183247 · 2019-03-14
Device Summary
Frequently Asked Questions
What is the dpl Faceware?
dpl Faceware is a medical device that received FDA 510(k) clearance on 2019-03-14. The listed applicant is Led Technologies, Inc.. The 510(k) number is K183247.
When did dpl Faceware receive FDA 510(k) clearance?
dpl Faceware received FDA 510(k) clearance on 2019-03-14, under 510(k) number K183247.
Who is the listed applicant for dpl Faceware?
The FDA 510(k) record lists Led Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for dpl Faceware?
The FDA product code for dpl Faceware is OHS.
Other records listing Led Technologies, 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: OHS)
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.