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FDA 510(k)

HOLOPSY SYSTEM

K-Number: K951999 · 1996-01-05

ApplicantNeovision Corp.
Decision Date1996-01-05
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HOLOPSY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Neovision Corp.. It received FDA 510(k) clearance on 1996-01-05 under 510(k) number K951999. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLOPSY SYSTEM?

HOLOPSY SYSTEM is a medical device that received FDA 510(k) clearance on 1996-01-05. The listed applicant is Neovision Corp.. The 510(k) number is K951999.

When did HOLOPSY SYSTEM receive FDA 510(k) clearance?

HOLOPSY SYSTEM received FDA 510(k) clearance on 1996-01-05, under 510(k) number K951999.

Who is the listed applicant for HOLOPSY SYSTEM?

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

What is the FDA product code for HOLOPSY SYSTEM?

The FDA product code for HOLOPSY SYSTEM is IYO.

Related Clinical Trials

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Other records listing Neovision Corp. 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.

K980423SONOPSY LA SYSTEM

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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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