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FDA 510(k)

PLASTIC DISPOSABLE BIB

K-Number: K761108 · 1976-12-02

Decision Date1976-12-02
Product CodeKME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLASTIC DISPOSABLE BIB 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 1976-12-02 under 510(k) number K761108. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC DISPOSABLE BIB?

PLASTIC DISPOSABLE BIB is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K761108.

When did PLASTIC DISPOSABLE BIB receive FDA 510(k) clearance?

PLASTIC DISPOSABLE BIB received FDA 510(k) clearance on 1976-12-02, under 510(k) number K761108.

Who is the listed applicant for PLASTIC DISPOSABLE BIB?

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 PLASTIC DISPOSABLE BIB?

The FDA product code for PLASTIC DISPOSABLE BIB is KME.

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: KME)

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

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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