SmartGrid
K-Number: K163157 · 2017-03-21
Device Summary
Frequently Asked Questions
What is the SmartGrid?
SmartGrid is a medical device that received FDA 510(k) clearance on 2017-03-21. The listed applicant is Carestream Health. The 510(k) number is K163157.
When did SmartGrid receive FDA 510(k) clearance?
SmartGrid received FDA 510(k) clearance on 2017-03-21, under 510(k) number K163157.
Who is the listed applicant for SmartGrid?
The FDA 510(k) record lists Carestream Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SmartGrid?
The FDA product code for SmartGrid is MQB.
Other records listing Carestream Health 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: MQB)
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.