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FDA 510(k)

ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000

K-Number: K852114 · 1985-09-27

Decision Date1985-09-27
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000 is the device name listed in this FDA 510(k) record. The listed applicant is Ars Enterprises, Inc.. It received FDA 510(k) clearance on 1985-09-27 under 510(k) number K852114. 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 ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000?

ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000 is a medical device that received FDA 510(k) clearance on 1985-09-27. The listed applicant is Ars Enterprises, Inc.. The 510(k) number is K852114.

When did ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000 receive FDA 510(k) clearance?

ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000 received FDA 510(k) clearance on 1985-09-27, under 510(k) number K852114.

Who is the listed applicant for ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000?

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

What is the FDA product code for ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000?

The FDA product code for ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000 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 Ars Enterprises, 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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