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FDA 510(k)

VIGIL II

K-Number: K920845 · 1992-12-07

ApplicantBeckman Instruments, Inc.
Decision Date1992-12-07
Product CodeDCK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

VIGIL II is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1992-12-07 under 510(k) number K920845. The device is classified under product code DCK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIGIL II?

VIGIL II is a medical device that received FDA 510(k) clearance on 1992-12-07. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K920845.

When did VIGIL II receive FDA 510(k) clearance?

VIGIL II received FDA 510(k) clearance on 1992-12-07, under 510(k) number K920845.

Who is the listed applicant for VIGIL II?

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

What is the FDA product code for VIGIL II?

The FDA product code for VIGIL II is DCK.

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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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