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FDA 510(k)

YOUNG D'GRANULATOR

K-Number: K932255 · 1994-04-15

Decision Date1994-04-15
Product CodeKMW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

YOUNG D'GRANULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Young Dental Manufacturing Co. 1, LLC. It received FDA 510(k) clearance on 1994-04-15 under 510(k) number K932255. The device is classified under product code KMW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YOUNG D'GRANULATOR?

YOUNG D'GRANULATOR is a medical device that received FDA 510(k) clearance on 1994-04-15. The listed applicant is Young Dental Manufacturing Co. 1, LLC. The 510(k) number is K932255.

When did YOUNG D'GRANULATOR receive FDA 510(k) clearance?

YOUNG D'GRANULATOR received FDA 510(k) clearance on 1994-04-15, under 510(k) number K932255.

Who is the listed applicant for YOUNG D'GRANULATOR?

The FDA 510(k) record lists Young Dental Manufacturing Co. 1, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YOUNG D'GRANULATOR?

The FDA product code for YOUNG D'GRANULATOR is KMW.

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 Young Dental Manufacturing Co. 1, LLC 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 16 devices →

Related Devices (Code: KMW)

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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