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FDA 510(k)

STERI-SHURE

K-Number: K820147 · 1982-02-05

ApplicantGeneral Health Systems, Inc.
Decision Date1982-02-05
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERI-SHURE is the device name listed in this FDA 510(k) record. The listed applicant is General Health Systems, Inc.. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820147. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-SHURE?

STERI-SHURE is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is General Health Systems, Inc.. The 510(k) number is K820147.

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

STERI-SHURE received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820147.

Who is the listed applicant for STERI-SHURE?

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

What is the FDA product code for STERI-SHURE?

The FDA product code for STERI-SHURE is JOJ.

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Related Devices (Code: JOJ)

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.

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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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