dpl II Panel
K-Number: K171390 · 2017-08-03
Device Summary
Frequently Asked Questions
What is the dpl II Panel?
dpl II Panel is a medical device that received FDA 510(k) clearance on 2017-08-03. The listed applicant is Led Technologies, Inc.. The 510(k) number is K171390.
When did dpl II Panel receive FDA 510(k) clearance?
dpl II Panel received FDA 510(k) clearance on 2017-08-03, under 510(k) number K171390.
Who is the listed applicant for dpl II Panel?
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 II Panel?
The FDA product code for dpl II Panel 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.