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

FDA 510(k)

ND3100 VIDEO IMAGER

K-Number: K843349 · 1984-12-17

Decision Date1984-12-17
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ND3100 VIDEO IMAGER is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Data, Inc.. It received FDA 510(k) clearance on 1984-12-17 under 510(k) number K843349. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ND3100 VIDEO IMAGER?

ND3100 VIDEO IMAGER is a medical device that received FDA 510(k) clearance on 1984-12-17. The listed applicant is Nuclear Data, Inc.. The 510(k) number is K843349.

When did ND3100 VIDEO IMAGER receive FDA 510(k) clearance?

ND3100 VIDEO IMAGER received FDA 510(k) clearance on 1984-12-17, under 510(k) number K843349.

Who is the listed applicant for ND3100 VIDEO IMAGER?

The FDA 510(k) record lists Nuclear Data, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ND3100 VIDEO IMAGER?

The FDA product code for ND3100 VIDEO IMAGER is LMB.

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 Nuclear Data, 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.

View all 7 devices →

Related Devices (Code: LMB)

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.

↑