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FDA 510(k)

STERIGAGE EO 100%

K-Number: K934874 · 1995-04-18

ApplicantPymah Corp.
Decision Date1995-04-18
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERIGAGE EO 100% is the device name listed in this FDA 510(k) record. The listed applicant is Pymah Corp.. It received FDA 510(k) clearance on 1995-04-18 under 510(k) number K934874. 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 STERIGAGE EO 100%?

STERIGAGE EO 100% is a medical device that received FDA 510(k) clearance on 1995-04-18. The listed applicant is Pymah Corp.. The 510(k) number is K934874.

When did STERIGAGE EO 100% receive FDA 510(k) clearance?

STERIGAGE EO 100% received FDA 510(k) clearance on 1995-04-18, under 510(k) number K934874.

Who is the listed applicant for STERIGAGE EO 100%?

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

What is the FDA product code for STERIGAGE EO 100%?

The FDA product code for STERIGAGE EO 100% is JOJ.

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Other records listing Pymah 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.

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Related Devices (Code: JOJ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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