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FDA 510(k)

SES-2012 AUTOMATIC STEAM STERILIZER

K-Number: K924596 · 1994-04-15

Decision Date1994-04-15
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SES-2012 AUTOMATIC STEAM STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Porter Instrument Co., Inc.. It received FDA 510(k) clearance on 1994-04-15 under 510(k) number K924596. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SES-2012 AUTOMATIC STEAM STERILIZER?

SES-2012 AUTOMATIC STEAM STERILIZER is a medical device that received FDA 510(k) clearance on 1994-04-15. The listed applicant is Porter Instrument Co., Inc.. The 510(k) number is K924596.

When did SES-2012 AUTOMATIC STEAM STERILIZER receive FDA 510(k) clearance?

SES-2012 AUTOMATIC STEAM STERILIZER received FDA 510(k) clearance on 1994-04-15, under 510(k) number K924596.

Who is the listed applicant for SES-2012 AUTOMATIC STEAM STERILIZER?

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

What is the FDA product code for SES-2012 AUTOMATIC STEAM STERILIZER?

The FDA product code for SES-2012 AUTOMATIC STEAM STERILIZER is FLE.

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 Porter Instrument Co., 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: FLE)

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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