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FDA 510(k)

TRAY DOUGH

K-Number: K911225 · 1991-04-17

Decision Date1991-04-17
Product CodeKGS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRAY DOUGH is the device name listed in this FDA 510(k) record. The listed applicant is The Hygenic Corp.. It received FDA 510(k) clearance on 1991-04-17 under 510(k) number K911225. The device is classified under product code KGS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAY DOUGH?

TRAY DOUGH is a medical device that received FDA 510(k) clearance on 1991-04-17. The listed applicant is The Hygenic Corp.. The 510(k) number is K911225.

When did TRAY DOUGH receive FDA 510(k) clearance?

TRAY DOUGH received FDA 510(k) clearance on 1991-04-17, under 510(k) number K911225.

Who is the listed applicant for TRAY DOUGH?

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

What is the FDA product code for TRAY DOUGH?

The FDA product code for TRAY DOUGH is KGS.

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 The Hygenic Corp. 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: KGS)

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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