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FDA 510(k)

MDT/CASTLE PURUS DENTAL UNIT

K-Number: K914697 · 1991-11-13

Decision Date1991-11-13
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MDT/CASTLE PURUS DENTAL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Corp., Inc.. It received FDA 510(k) clearance on 1991-11-13 under 510(k) number K914697. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT/CASTLE PURUS DENTAL UNIT?

MDT/CASTLE PURUS DENTAL UNIT is a medical device that received FDA 510(k) clearance on 1991-11-13. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K914697.

When did MDT/CASTLE PURUS DENTAL UNIT receive FDA 510(k) clearance?

MDT/CASTLE PURUS DENTAL UNIT received FDA 510(k) clearance on 1991-11-13, under 510(k) number K914697.

Who is the listed applicant for MDT/CASTLE PURUS DENTAL UNIT?

The FDA 510(k) record lists Mdt Corp., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDT/CASTLE PURUS DENTAL UNIT?

The FDA product code for MDT/CASTLE PURUS DENTAL UNIT is EIA.

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 Mdt Corp., 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.

View all 22 devices →

Related Devices (Code: EIA)

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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