SHORTSTOP DISPOSABLE PROPHY ANGLE
K-Number: K955654 · 1996-02-08
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Device Summary
Frequently Asked Questions
What is the SHORTSTOP DISPOSABLE PROPHY ANGLE?
SHORTSTOP DISPOSABLE PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 1996-02-08. The listed applicant is Spintech, Inc.. The 510(k) number is K955654.
When did SHORTSTOP DISPOSABLE PROPHY ANGLE receive FDA 510(k) clearance?
SHORTSTOP DISPOSABLE PROPHY ANGLE received FDA 510(k) clearance on 1996-02-08, under 510(k) number K955654.
Who is the listed applicant for SHORTSTOP DISPOSABLE PROPHY ANGLE?
The FDA 510(k) record lists Spintech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHORTSTOP DISPOSABLE PROPHY ANGLE?
The FDA product code for SHORTSTOP DISPOSABLE PROPHY ANGLE is EFB.
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 Spintech, 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: EFB)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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