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FDA 510(k)

STERI-VERS

K-Number: K810311 · 1981-04-17

ApplicantThe Hilrad Co.
Decision Date1981-04-17
Product CodeLDS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERI-VERS is the device name listed in this FDA 510(k) record. The listed applicant is The Hilrad Co.. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K810311. The device is classified under product code LDS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-VERS?

STERI-VERS is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is The Hilrad Co.. The 510(k) number is K810311.

When did STERI-VERS receive FDA 510(k) clearance?

STERI-VERS received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810311.

Who is the listed applicant for STERI-VERS?

The FDA 510(k) record lists The Hilrad Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERI-VERS?

The FDA product code for STERI-VERS is LDS.

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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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