Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NDOHD High Definition Imaging System (NDOHD)

K-Number: K190420 · 2019-04-15

Decision Date2019-04-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NDOHD High Definition Imaging System (NDOHD) is a medical device manufactured by Altaravision, Inc.. It received FDA 510(k) clearance on 2019-04-15 under approval number K190420. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NDOHD High Definition Imaging System (NDOHD)?

NDOHD High Definition Imaging System (NDOHD) is a medical device that received FDA 510(k) clearance on 2019-04-15. It is manufactured by Altaravision, Inc.. The 510(k) number is K190420.

When was NDOHD High Definition Imaging System (NDOHD) approved by the FDA?

NDOHD High Definition Imaging System (NDOHD) received FDA 510(k) clearance on 2019-04-15, under approval number K190420.

What company makes NDOHD High Definition Imaging System (NDOHD)?

NDOHD High Definition Imaging System (NDOHD) is manufactured by Altaravision, Inc..

What is the FDA product code for NDOHD High Definition Imaging System (NDOHD)?

The FDA product code for NDOHD High Definition Imaging System (NDOHD) is LLZ.

Related Clinical Trials

Related PubMed Literature

Related Devices (Code: LLZ)

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.