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FDA 510(k)

VFI/VFE SYSTEM II

K-Number: K854872 · 1986-02-13

ApplicantMira, Inc.
Decision Date1986-02-13
Product Code
DecisionSubstantially Equivalent

Device Summary

VFI/VFE SYSTEM II is the device name listed in this FDA 510(k) record. The listed applicant is Mira, Inc.. It received FDA 510(k) clearance on 1986-02-13 under 510(k) number K854872. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VFI/VFE SYSTEM II?

VFI/VFE SYSTEM II is a medical device that received FDA 510(k) clearance on 1986-02-13. The listed applicant is Mira, Inc.. The 510(k) number is K854872.

When did VFI/VFE SYSTEM II receive FDA 510(k) clearance?

VFI/VFE SYSTEM II received FDA 510(k) clearance on 1986-02-13, under 510(k) number K854872.

Who is the listed applicant for VFI/VFE SYSTEM II?

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

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Other records listing Mira, 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.

K951728SCHEPENS-YOSHIDA VIDEO BINOCULAR INDIRECT OPHTHALMSCOPEK950806SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTSK941495RETURN PATH DIATHERMY HANDLEK933527MODIFICATION OF ANTERIOR SEGMENT ELECTRODESK923629OPHTHALMIC TRICHIASIS PROBEK894248CONVERTER SYSTEM

View all 21 devices →

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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