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FDA 510(k)

SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS

K-Number: K951065 · 1995-06-08

Decision Date1995-06-08
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Steri-Oss, Inc.. It received FDA 510(k) clearance on 1995-06-08 under 510(k) number K951065. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS?

SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS is a medical device that received FDA 510(k) clearance on 1995-06-08. The listed applicant is Steri-Oss, Inc.. The 510(k) number is K951065.

When did SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS receive FDA 510(k) clearance?

SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS received FDA 510(k) clearance on 1995-06-08, under 510(k) number K951065.

Who is the listed applicant for SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS?

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

What is the FDA product code for SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS?

The FDA product code for SURGICAL INSTRUMENT MOTOTRS AND ACCESSORIES/ATTACHMENTS is DZE.

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 Steri-Oss, 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.

View all 46 devices →

Related Devices (Code: DZE)

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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