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FDA 510(k)

EATING UTENSILS

K-Number: K821643 · 1982-06-11

ApplicantFred Sammons, Inc.
Decision Date1982-06-11
Product CodeILC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EATING UTENSILS is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1982-06-11 under 510(k) number K821643. The device is classified under product code ILC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EATING UTENSILS?

EATING UTENSILS is a medical device that received FDA 510(k) clearance on 1982-06-11. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K821643.

When did EATING UTENSILS receive FDA 510(k) clearance?

EATING UTENSILS received FDA 510(k) clearance on 1982-06-11, under 510(k) number K821643.

Who is the listed applicant for EATING UTENSILS?

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

What is the FDA product code for EATING UTENSILS?

The FDA product code for EATING UTENSILS is ILC.

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Other records listing Fred Sammons, 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.

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Related Devices (Code: ILC)

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.

K833177GLOSSECTOMY FEEDING SPOONSMaddak, Inc.K830854COLLAPSABLE LAVATORY SEAT HEIGHTENERLic-OrthionK830851BATH TUB SEAT & BATH BOARDLic-OrthionK823594PLASTIC BUILT-UP HANDLE EATING UTENSILSFred Sammons, Inc.K813630BK-1129 BOTTLE STRAWFred Sammons, Inc.K812346ALUMINUM SCOOP DISKFred Sammons, Inc.

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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