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)

VISIONLINK ACR-NEMA CONVERSION UTILITIES

K-Number: K935103 · 1994-02-09

Decision Date1994-02-09
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISIONLINK ACR-NEMA CONVERSION UTILITIES is the device name listed in this FDA 510(k) record. The listed applicant is Evergreen Technologies, Inc.. It received FDA 510(k) clearance on 1994-02-09 under 510(k) number K935103. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISIONLINK ACR-NEMA CONVERSION UTILITIES?

VISIONLINK ACR-NEMA CONVERSION UTILITIES is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Evergreen Technologies, Inc.. The 510(k) number is K935103.

When did VISIONLINK ACR-NEMA CONVERSION UTILITIES receive FDA 510(k) clearance?

VISIONLINK ACR-NEMA CONVERSION UTILITIES received FDA 510(k) clearance on 1994-02-09, under 510(k) number K935103.

Who is the listed applicant for VISIONLINK ACR-NEMA CONVERSION UTILITIES?

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

What is the FDA product code for VISIONLINK ACR-NEMA CONVERSION UTILITIES?

The FDA product code for VISIONLINK ACR-NEMA CONVERSION UTILITIES is LMD.

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 Evergreen 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.

View all 7 devices →

Related Devices (Code: LMD)

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.

↑