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FDA 510(k)

KNIFE, ROCKER, SLOTTED HANDLE

K-Number: K781192 · 1978-07-31

Decision Date1978-07-31
Product CodeILC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KNIFE, ROCKER, SLOTTED HANDLE 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 1978-07-31 under 510(k) number K781192. 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 KNIFE, ROCKER, SLOTTED HANDLE?

KNIFE, ROCKER, SLOTTED HANDLE is a medical device that received FDA 510(k) clearance on 1978-07-31. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K781192.

When did KNIFE, ROCKER, SLOTTED HANDLE receive FDA 510(k) clearance?

KNIFE, ROCKER, SLOTTED HANDLE received FDA 510(k) clearance on 1978-07-31, under 510(k) number K781192.

Who is the listed applicant for KNIFE, ROCKER, SLOTTED HANDLE?

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 KNIFE, ROCKER, SLOTTED HANDLE?

The FDA product code for KNIFE, ROCKER, SLOTTED HANDLE is ILC.

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 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.

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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