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)

IMAGE PROCESSING SYS A3

K-Number: K832505 · 1983-09-12

Decision Date1983-09-12
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGE PROCESSING SYS A3 is the device name listed in this FDA 510(k) record. The listed applicant is Metronic, Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832505. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGE PROCESSING SYS A3?

IMAGE PROCESSING SYS A3 is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Metronic, Inc.. The 510(k) number is K832505.

When did IMAGE PROCESSING SYS A3 receive FDA 510(k) clearance?

IMAGE PROCESSING SYS A3 received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832505.

Who is the listed applicant for IMAGE PROCESSING SYS A3?

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

What is the FDA product code for IMAGE PROCESSING SYS A3?

The FDA product code for IMAGE PROCESSING SYS A3 is IYX.

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 Metronic, 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.

Related Devices (Code: IYX)

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.

↑