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FDA 510(k)

WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM

K-Number: K925829 · 1993-02-12

Decision Date1993-02-12
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Waggoner Dental Mfg.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K925829. 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 WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM?

WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Waggoner Dental Mfg.. The 510(k) number is K925829.

When did WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM receive FDA 510(k) clearance?

WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM received FDA 510(k) clearance on 1993-02-12, under 510(k) number K925829.

Who is the listed applicant for WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM?

The FDA 510(k) record lists Waggoner Dental Mfg. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM?

The FDA product code for WAGGONER DENTAL MANUFACTURING STERIWATER SYSTEM 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.

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

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