DISPOSABLE PROPHY ANGLE; DISPOSABLE PROPHY ANGLE
K-Number: K103157 · 2011-01-24
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE PROPHY ANGLE; DISPOSABLE PROPHY ANGLE?
DISPOSABLE PROPHY ANGLE; DISPOSABLE PROPHY ANGLE is a medical device that received FDA 510(k) clearance on 2011-01-24. The listed applicant is Angstrom Mfg., Inc.. The 510(k) number is K103157.
When did DISPOSABLE PROPHY ANGLE; DISPOSABLE PROPHY ANGLE receive FDA 510(k) clearance?
DISPOSABLE PROPHY ANGLE; DISPOSABLE PROPHY ANGLE received FDA 510(k) clearance on 2011-01-24, under 510(k) number K103157.
Who is the listed applicant for DISPOSABLE PROPHY ANGLE; DISPOSABLE PROPHY ANGLE?
The FDA 510(k) record lists Angstrom Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE PROPHY ANGLE; DISPOSABLE PROPHY ANGLE?
The FDA product code for DISPOSABLE PROPHY ANGLE; 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 Angstrom Mfg., 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
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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