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FDA 510(k)

ALUMINUM SCOOP DISK

K-Number: K812346 · 1981-09-11

ApplicantFred Sammons, Inc.
Decision Date1981-09-11
Product CodeILC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ALUMINUM SCOOP DISK 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 1981-09-11 under 510(k) number K812346. 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 ALUMINUM SCOOP DISK?

ALUMINUM SCOOP DISK is a medical device that received FDA 510(k) clearance on 1981-09-11. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K812346.

When did ALUMINUM SCOOP DISK receive FDA 510(k) clearance?

ALUMINUM SCOOP DISK received FDA 510(k) clearance on 1981-09-11, under 510(k) number K812346.

Who is the listed applicant for ALUMINUM SCOOP DISK?

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 ALUMINUM SCOOP DISK?

The FDA product code for ALUMINUM SCOOP DISK is ILC.

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Other records listing Fred Sammons, Inc. as applicant

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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.K821643EATING UTENSILSFred Sammons, Inc.K813630BK-1129 BOTTLE STRAWFred 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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