M4 CONTRA-ANGLE HANDPIECE
K-Number: K942480 · 1995-01-27
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Device Summary
Frequently Asked Questions
What is the M4 CONTRA-ANGLE HANDPIECE?
M4 CONTRA-ANGLE HANDPIECE is a medical device that received FDA 510(k) clearance on 1995-01-27. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K942480.
When did M4 CONTRA-ANGLE HANDPIECE receive FDA 510(k) clearance?
M4 CONTRA-ANGLE HANDPIECE received FDA 510(k) clearance on 1995-01-27, under 510(k) number K942480.
Who is the listed applicant for M4 CONTRA-ANGLE HANDPIECE?
The FDA 510(k) record lists Kerr Corporation (Danbury) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for M4 CONTRA-ANGLE HANDPIECE?
The FDA product code for M4 CONTRA-ANGLE HANDPIECE 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 Kerr Corporation (Danbury) 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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