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FDA 510(k)

RHESUS SV5/SV40

K-Number: K841665 · 1984-05-07

ApplicantViromed Laboratories, Inc.
Decision Date1984-05-07
Product CodeKIR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RHESUS SV5/SV40 is the device name listed in this FDA 510(k) record. The listed applicant is Viromed Laboratories, Inc.. It received FDA 510(k) clearance on 1984-05-07 under 510(k) number K841665. The device is classified under product code KIR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHESUS SV5/SV40?

RHESUS SV5/SV40 is a medical device that received FDA 510(k) clearance on 1984-05-07. The listed applicant is Viromed Laboratories, Inc.. The 510(k) number is K841665.

When did RHESUS SV5/SV40 receive FDA 510(k) clearance?

RHESUS SV5/SV40 received FDA 510(k) clearance on 1984-05-07, under 510(k) number K841665.

Who is the listed applicant for RHESUS SV5/SV40?

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

What is the FDA product code for RHESUS SV5/SV40?

The FDA product code for RHESUS SV5/SV40 is KIR.

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Related Devices (Code: KIR)

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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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