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FDA 510(k)

CHLAMYDIA OVERBY MEDIA

K-Number: K831686 · 1983-07-07

ApplicantViromed Laboratories, Inc.
Decision Date1983-07-07
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CHLAMYDIA OVERBY MEDIA 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 1983-07-07 under 510(k) number K831686. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHLAMYDIA OVERBY MEDIA?

CHLAMYDIA OVERBY MEDIA is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is Viromed Laboratories, Inc.. The 510(k) number is K831686.

When did CHLAMYDIA OVERBY MEDIA receive FDA 510(k) clearance?

CHLAMYDIA OVERBY MEDIA received FDA 510(k) clearance on 1983-07-07, under 510(k) number K831686.

Who is the listed applicant for CHLAMYDIA OVERBY MEDIA?

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 CHLAMYDIA OVERBY MEDIA?

The FDA product code for CHLAMYDIA OVERBY MEDIA is KIT.

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Related Devices (Code: KIT)

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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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