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FDA 510(k)

MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881

K-Number: K031799 · 2003-11-12

ApplicantMiele, Inc.
Decision Date2003-11-12
Product CodeLDS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881 is the device name listed in this FDA 510(k) record. The listed applicant is Miele, Inc.. It received FDA 510(k) clearance on 2003-11-12 under 510(k) number K031799. The device is classified under product code LDS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881?

MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881 is a medical device that received FDA 510(k) clearance on 2003-11-12. The listed applicant is Miele, Inc.. The 510(k) number is K031799.

When did MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881 receive FDA 510(k) clearance?

MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881 received FDA 510(k) clearance on 2003-11-12, under 510(k) number K031799.

Who is the listed applicant for MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881?

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

What is the FDA product code for MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881?

The FDA product code for MIELE DENTAL THERMAL DISINFECTOR, MODEL G7881 is LDS.

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: LDS)

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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