ROTORY SCALER SWIVEL IMPROVEMENT FEATURE, TITAN SW
K-Number: K881253 · 1988-04-21
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Device Summary
Frequently Asked Questions
What is the ROTORY SCALER SWIVEL IMPROVEMENT FEATURE, TITAN SW?
ROTORY SCALER SWIVEL IMPROVEMENT FEATURE, TITAN SW is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Dentalez Group. The 510(k) number is K881253.
When did ROTORY SCALER SWIVEL IMPROVEMENT FEATURE, TITAN SW receive FDA 510(k) clearance?
ROTORY SCALER SWIVEL IMPROVEMENT FEATURE, TITAN SW received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881253.
Who is the listed applicant for ROTORY SCALER SWIVEL IMPROVEMENT FEATURE, TITAN SW?
The FDA 510(k) record lists Dentalez Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROTORY SCALER SWIVEL IMPROVEMENT FEATURE, TITAN SW?
The FDA product code for ROTORY SCALER SWIVEL IMPROVEMENT FEATURE, TITAN SW is ELC.
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 Dentalez Group 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: ELC)
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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