COLTENE PRESIDENT JET REGULAR BODY
K-Number: K882800 · 1988-09-23
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Device Summary
Frequently Asked Questions
What is the COLTENE PRESIDENT JET REGULAR BODY?
COLTENE PRESIDENT JET REGULAR BODY is a medical device that received FDA 510(k) clearance on 1988-09-23. The listed applicant is Coltene, Inc.. The 510(k) number is K882800.
When did COLTENE PRESIDENT JET REGULAR BODY receive FDA 510(k) clearance?
COLTENE PRESIDENT JET REGULAR BODY received FDA 510(k) clearance on 1988-09-23, under 510(k) number K882800.
Who is the listed applicant for COLTENE PRESIDENT JET REGULAR BODY?
The FDA 510(k) record lists Coltene, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLTENE PRESIDENT JET REGULAR BODY?
The FDA product code for COLTENE PRESIDENT JET REGULAR BODY is ELW.
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 Coltene, 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: ELW)
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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