FDA 510(k)

VFC UNIT

K-Number: K920746 · 1992-06-30

Decision Date1992-06-30

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

VFC UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Tilane Corp.. It received FDA 510(k) clearance on 1992-06-30 under 510(k) number K920746. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VFC UNIT?

VFC UNIT is a medical device that received FDA 510(k) clearance on 1992-06-30. The listed applicant is Tilane Corp.. The 510(k) number is K920746.

When did VFC UNIT receive FDA 510(k) clearance?

VFC UNIT received FDA 510(k) clearance on 1992-06-30, under 510(k) number K920746.

Who is the listed applicant for VFC UNIT?

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

What is the FDA product code for VFC UNIT?

The FDA product code for VFC UNIT is JAA.

Other records listing Tilane 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.

K964322VIPOR UNIT

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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.