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)

DIGITAL IMAGE PROCESSOR FP-2C

K-Number: K850080 · 1985-04-19

ApplicantEigen Video
Decision Date1985-04-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL IMAGE PROCESSOR FP-2C is the device name listed in this FDA 510(k) record. The listed applicant is Eigen Video. It received FDA 510(k) clearance on 1985-04-19 under 510(k) number K850080. 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 DIGITAL IMAGE PROCESSOR FP-2C?

DIGITAL IMAGE PROCESSOR FP-2C is a medical device that received FDA 510(k) clearance on 1985-04-19. The listed applicant is Eigen Video. The 510(k) number is K850080.

When did DIGITAL IMAGE PROCESSOR FP-2C receive FDA 510(k) clearance?

DIGITAL IMAGE PROCESSOR FP-2C received FDA 510(k) clearance on 1985-04-19, under 510(k) number K850080.

Who is the listed applicant for DIGITAL IMAGE PROCESSOR FP-2C?

The FDA 510(k) record lists Eigen Video as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL IMAGE PROCESSOR FP-2C?

The FDA product code for DIGITAL IMAGE PROCESSOR FP-2C is LLZ.

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 Eigen Video 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: LLZ)

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.

↑