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FDA 510(k)

STAT ULTRA VIOLET LIQUID

K-Number: K781432 · 1978-10-03

ApplicantBeckman Instruments, Inc.
Decision Date1978-10-03
Product CodeJHS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

STAT ULTRA VIOLET LIQUID 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 1978-10-03 under 510(k) number K781432. The device is classified under product code JHS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAT ULTRA VIOLET LIQUID?

STAT ULTRA VIOLET LIQUID is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K781432.

When did STAT ULTRA VIOLET LIQUID receive FDA 510(k) clearance?

STAT ULTRA VIOLET LIQUID received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781432.

Who is the listed applicant for STAT ULTRA VIOLET LIQUID?

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 STAT ULTRA VIOLET LIQUID?

The FDA product code for STAT ULTRA VIOLET LIQUID is JHS.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: JHS)

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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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