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FDA 510(k)

CONTROL SERUMS FOR NONTREPONEMAL TEST

K-Number: K810119 · 1981-02-09

ApplicantHillside Acres, Inc.
Decision Date1981-02-09
Product CodeGMP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CONTROL SERUMS FOR NONTREPONEMAL TEST is the device name listed in this FDA 510(k) record. The listed applicant is Hillside Acres, Inc.. It received FDA 510(k) clearance on 1981-02-09 under 510(k) number K810119. The device is classified under product code GMP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTROL SERUMS FOR NONTREPONEMAL TEST?

CONTROL SERUMS FOR NONTREPONEMAL TEST is a medical device that received FDA 510(k) clearance on 1981-02-09. The listed applicant is Hillside Acres, Inc.. The 510(k) number is K810119.

When did CONTROL SERUMS FOR NONTREPONEMAL TEST receive FDA 510(k) clearance?

CONTROL SERUMS FOR NONTREPONEMAL TEST received FDA 510(k) clearance on 1981-02-09, under 510(k) number K810119.

Who is the listed applicant for CONTROL SERUMS FOR NONTREPONEMAL TEST?

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

What is the FDA product code for CONTROL SERUMS FOR NONTREPONEMAL TEST?

The FDA product code for CONTROL SERUMS FOR NONTREPONEMAL TEST is GMP.

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Related Devices (Code: GMP)

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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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