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FDA 510(k)

THERMALOG S STEAM STERILIZATION INTEGRA

K-Number: K813202 · 1981-12-31

Decision Date1981-12-31
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THERMALOG S STEAM STERILIZATION INTEGRA is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Medical Sciences, Inc.. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813202. 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 THERMALOG S STEAM STERILIZATION INTEGRA?

THERMALOG S STEAM STERILIZATION INTEGRA is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Bio-Medical Sciences, Inc.. The 510(k) number is K813202.

When did THERMALOG S STEAM STERILIZATION INTEGRA receive FDA 510(k) clearance?

THERMALOG S STEAM STERILIZATION INTEGRA received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813202.

Who is the listed applicant for THERMALOG S STEAM STERILIZATION INTEGRA?

The FDA 510(k) record lists Bio-Medical Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERMALOG S STEAM STERILIZATION INTEGRA?

The FDA product code for THERMALOG S STEAM STERILIZATION INTEGRA is JOJ.

Related Clinical Trials

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.

Other records listing Bio-Medical Sciences, Inc. 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.

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.

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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