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FDA 510(k)

ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE

K-Number: K023953 · 2003-02-14

Decision Date2003-02-14
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is St. George Technology, Inc.. It received FDA 510(k) clearance on 2003-02-14 under 510(k) number K023953. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE?

ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 2003-02-14. The listed applicant is St. George Technology, Inc.. The 510(k) number is K023953.

When did ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE receive FDA 510(k) clearance?

ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE received FDA 510(k) clearance on 2003-02-14, under 510(k) number K023953.

Who is the listed applicant for ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE?

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

What is the FDA product code for ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE?

The FDA product code for ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE is EGS.

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 St. George Technology, 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: EGS)

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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