DENTAL INSTRUMENTS CURETTE PERIODONTAL
K-Number: K931329 · 1994-01-27
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Device Summary
Frequently Asked Questions
What is the DENTAL INSTRUMENTS CURETTE PERIODONTAL?
DENTAL INSTRUMENTS CURETTE PERIODONTAL is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Minnesota Prophy Power, Inc.. The 510(k) number is K931329.
When did DENTAL INSTRUMENTS CURETTE PERIODONTAL receive FDA 510(k) clearance?
DENTAL INSTRUMENTS CURETTE PERIODONTAL received FDA 510(k) clearance on 1994-01-27, under 510(k) number K931329.
Who is the listed applicant for DENTAL INSTRUMENTS CURETTE PERIODONTAL?
The FDA 510(k) record lists Minnesota Prophy Power, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTAL INSTRUMENTS CURETTE PERIODONTAL?
The FDA product code for DENTAL INSTRUMENTS CURETTE PERIODONTAL is EMS.
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 Minnesota Prophy Power, 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: EMS)
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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