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FDA 510(k)

DENTAL INSTRUMENTS CURETTE PERIODONTAL

K-Number: K931329 · 1994-01-27

Decision Date1994-01-27
Product CodeEMS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL INSTRUMENTS CURETTE PERIODONTAL is the device name listed in this FDA 510(k) record. The listed applicant is Minnesota Prophy Power, Inc.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K931329. The device is classified under product code EMS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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