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FDA 510(k)

CARDS, GIANT FACE PLAYING BK-9419

K-Number: K760306 · 1976-09-08

Decision Date1976-09-08
Product CodeILT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CARDS, GIANT FACE PLAYING BK-9419 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 1976-09-08 under 510(k) number K760306. The device is classified under product code ILT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDS, GIANT FACE PLAYING BK-9419?

CARDS, GIANT FACE PLAYING BK-9419 is a medical device that received FDA 510(k) clearance on 1976-09-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K760306.

When did CARDS, GIANT FACE PLAYING BK-9419 receive FDA 510(k) clearance?

CARDS, GIANT FACE PLAYING BK-9419 received FDA 510(k) clearance on 1976-09-08, under 510(k) number K760306.

Who is the listed applicant for CARDS, GIANT FACE PLAYING BK-9419?

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 CARDS, GIANT FACE PLAYING BK-9419?

The FDA product code for CARDS, GIANT FACE PLAYING BK-9419 is ILT.

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.

View all 278 devices →

Related Devices (Code: ILT)

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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