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FDA 510(k)

JOSLYN EO STERILIZER/ EO MODERNIZATION KIT

K-Number: K901146 · 1991-03-07

Decision Date1991-03-07
Product CodeFLF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JOSLYN EO STERILIZER/ EO MODERNIZATION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Joslyn Valve Corp.. It received FDA 510(k) clearance on 1991-03-07 under 510(k) number K901146. The device is classified under product code FLF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOSLYN EO STERILIZER/ EO MODERNIZATION KIT?

JOSLYN EO STERILIZER/ EO MODERNIZATION KIT is a medical device that received FDA 510(k) clearance on 1991-03-07. The listed applicant is Joslyn Valve Corp.. The 510(k) number is K901146.

When did JOSLYN EO STERILIZER/ EO MODERNIZATION KIT receive FDA 510(k) clearance?

JOSLYN EO STERILIZER/ EO MODERNIZATION KIT received FDA 510(k) clearance on 1991-03-07, under 510(k) number K901146.

Who is the listed applicant for JOSLYN EO STERILIZER/ EO MODERNIZATION KIT?

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

What is the FDA product code for JOSLYN EO STERILIZER/ EO MODERNIZATION KIT?

The FDA product code for JOSLYN EO STERILIZER/ EO MODERNIZATION KIT is FLF.

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 Joslyn Valve 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.

Related Devices (Code: FLF)

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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