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FDA 510(k)

CORNEOMAP 4500 ULTRASOUND MEASUREMENT

K-Number: K837331 · 1983-05-09

ApplicantRadionics Medical, Inc.
Decision Date1983-05-09
Product Code
DecisionSubstantially Equivalent

Device Summary

CORNEOMAP 4500 ULTRASOUND MEASUREMENT is the device name listed in this FDA 510(k) record. The listed applicant is Radionics Medical, Inc.. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K837331. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORNEOMAP 4500 ULTRASOUND MEASUREMENT?

CORNEOMAP 4500 ULTRASOUND MEASUREMENT is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Radionics Medical, Inc.. The 510(k) number is K837331.

When did CORNEOMAP 4500 ULTRASOUND MEASUREMENT receive FDA 510(k) clearance?

CORNEOMAP 4500 ULTRASOUND MEASUREMENT received FDA 510(k) clearance on 1983-05-09, under 510(k) number K837331.

Who is the listed applicant for CORNEOMAP 4500 ULTRASOUND MEASUREMENT?

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

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.

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Other records listing Radionics Medical, 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.

K844299CORNEOMAP 4500K833222SINUSVU 2500K827035OCULAR BIOMETER 4000K810851SPECTRUM ANALYZER 8000

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.

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