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FDA 510(k)

BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER

K-Number: K951273 · 1995-08-08

ApplicantBuxton Medical Servic Corp.
Decision Date1995-08-08
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Buxton Medical Servic Corp.. It received FDA 510(k) clearance on 1995-08-08 under 510(k) number K951273. 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 BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER?

BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER is a medical device that received FDA 510(k) clearance on 1995-08-08. The listed applicant is Buxton Medical Servic Corp.. The 510(k) number is K951273.

When did BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER receive FDA 510(k) clearance?

BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER received FDA 510(k) clearance on 1995-08-08, under 510(k) number K951273.

Who is the listed applicant for BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER?

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

What is the FDA product code for BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER?

The FDA product code for BUXTON BUILT STERILIZER, BUXTON BUILT RECONDITIONED STERILIZER is FLE.

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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.

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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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