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FDA 510(k)

Q3 DISPOSABLE PROPHY ANGLE

K-Number: K923980 · 1993-05-27

Decision Date1993-05-27
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Q3 DISPOSABLE PROPHY ANGLE is the device name listed in this FDA 510(k) record. The listed applicant is Q3 Special Products, Inc.. It received FDA 510(k) clearance on 1993-05-27 under 510(k) number K923980. 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 Q3 DISPOSABLE PROPHY ANGLE?

Q3 DISPOSABLE PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 1993-05-27. The listed applicant is Q3 Special Products, Inc.. The 510(k) number is K923980.

When did Q3 DISPOSABLE PROPHY ANGLE receive FDA 510(k) clearance?

Q3 DISPOSABLE PROPHY ANGLE received FDA 510(k) clearance on 1993-05-27, under 510(k) number K923980.

Who is the listed applicant for Q3 DISPOSABLE PROPHY ANGLE?

The FDA 510(k) record lists Q3 Special Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q3 DISPOSABLE PROPHY ANGLE?

The FDA product code for Q3 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.

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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