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FDA 510(k)

SCOTT CM42 PASTEURIZER

K-Number: K810065 · 1981-01-28

ApplicantWilliam Harvey Life Products Corp.
Decision Date1981-01-28
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SCOTT CM42 PASTEURIZER is the device name listed in this FDA 510(k) record. The listed applicant is William Harvey Life Products Corp.. It received FDA 510(k) clearance on 1981-01-28 under 510(k) number K810065. 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 SCOTT CM42 PASTEURIZER?

SCOTT CM42 PASTEURIZER is a medical device that received FDA 510(k) clearance on 1981-01-28. The listed applicant is William Harvey Life Products Corp.. The 510(k) number is K810065.

When did SCOTT CM42 PASTEURIZER receive FDA 510(k) clearance?

SCOTT CM42 PASTEURIZER received FDA 510(k) clearance on 1981-01-28, under 510(k) number K810065.

Who is the listed applicant for SCOTT CM42 PASTEURIZER?

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

What is the FDA product code for SCOTT CM42 PASTEURIZER?

The FDA product code for SCOTT CM42 PASTEURIZER is HGX.

Related Clinical Trials

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Other records listing William Harvey Life Products Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K811703CARDIFF ALDASORBER SYSTEMK770720TUBING PACK, EXTRACORPOREAL, H-3000

Related Devices (Code: HGX)

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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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