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FDA 510(k)

EPISCLERAL VENOUS PRESSURE

K-Number: K843354 · 1984-11-19

ApplicantEyetech, LLC
Decision Date1984-11-19
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EPISCLERAL VENOUS PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is Eyetech, LLC. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K843354. The device is classified under product code HKX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPISCLERAL VENOUS PRESSURE?

EPISCLERAL VENOUS PRESSURE is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is Eyetech, LLC. The 510(k) number is K843354.

When did EPISCLERAL VENOUS PRESSURE receive FDA 510(k) clearance?

EPISCLERAL VENOUS PRESSURE received FDA 510(k) clearance on 1984-11-19, under 510(k) number K843354.

Who is the listed applicant for EPISCLERAL VENOUS PRESSURE?

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

What is the FDA product code for EPISCLERAL VENOUS PRESSURE?

The FDA product code for EPISCLERAL VENOUS PRESSURE is HKX.

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Related Devices (Code: HKX)

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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