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FDA 510(k)

OXFORD HUMAN MILK PASTEURISER

K-Number: K801246 · 1980-10-03

ApplicantVickers America Medical Corp.
Decision Date1980-10-03
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OXFORD HUMAN MILK PASTEURISER is the device name listed in this FDA 510(k) record. The listed applicant is Vickers America Medical Corp.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K801246. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXFORD HUMAN MILK PASTEURISER?

OXFORD HUMAN MILK PASTEURISER is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K801246.

When did OXFORD HUMAN MILK PASTEURISER receive FDA 510(k) clearance?

OXFORD HUMAN MILK PASTEURISER received FDA 510(k) clearance on 1980-10-03, under 510(k) number K801246.

Who is the listed applicant for OXFORD HUMAN MILK PASTEURISER?

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

What is the FDA product code for OXFORD HUMAN MILK PASTEURISER?

The FDA product code for OXFORD HUMAN MILK PASTEURISER is HGX.

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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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