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FDA 510(k)

VIGIL MULTICHEK CONTROLS

K-Number: K951170 · 1995-04-20

ApplicantBeckman Instruments, Inc.
Decision Date1995-04-20
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VIGIL MULTICHEK CONTROLS 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 1995-04-20 under 510(k) number K951170. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIGIL MULTICHEK CONTROLS?

VIGIL MULTICHEK CONTROLS is a medical device that received FDA 510(k) clearance on 1995-04-20. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K951170.

When did VIGIL MULTICHEK CONTROLS receive FDA 510(k) clearance?

VIGIL MULTICHEK CONTROLS received FDA 510(k) clearance on 1995-04-20, under 510(k) number K951170.

Who is the listed applicant for VIGIL MULTICHEK CONTROLS?

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 MULTICHEK CONTROLS?

The FDA product code for VIGIL MULTICHEK CONTROLS is JJY.

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Related Devices (Code: JJY)

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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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