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FDA 510(k)

ASEPTIC FLUID TRANSFER SYSTEM

K-Number: K830811 · 1983-04-28

ApplicantSteridoc Corp.
Decision Date1983-04-28
Product CodeKQQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ASEPTIC FLUID TRANSFER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Steridoc Corp.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K830811. The device is classified under product code KQQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASEPTIC FLUID TRANSFER SYSTEM?

ASEPTIC FLUID TRANSFER SYSTEM is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Steridoc Corp.. The 510(k) number is K830811.

When did ASEPTIC FLUID TRANSFER SYSTEM receive FDA 510(k) clearance?

ASEPTIC FLUID TRANSFER SYSTEM received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830811.

Who is the listed applicant for ASEPTIC FLUID TRANSFER SYSTEM?

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

What is the FDA product code for ASEPTIC FLUID TRANSFER SYSTEM?

The FDA product code for ASEPTIC FLUID TRANSFER SYSTEM is KQQ.

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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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