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FDA 510(k)

BONNER BRACE

K-Number: K810024 · 1981-01-23

ApplicantBee Ent.
Decision Date1981-01-23
Product CodeIQK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BONNER BRACE is the device name listed in this FDA 510(k) record. The listed applicant is Bee Ent.. It received FDA 510(k) clearance on 1981-01-23 under 510(k) number K810024. The device is classified under product code IQK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONNER BRACE?

BONNER BRACE is a medical device that received FDA 510(k) clearance on 1981-01-23. The listed applicant is Bee Ent.. The 510(k) number is K810024.

When did BONNER BRACE receive FDA 510(k) clearance?

BONNER BRACE received FDA 510(k) clearance on 1981-01-23, under 510(k) number K810024.

Who is the listed applicant for BONNER BRACE?

The FDA 510(k) record lists Bee Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BONNER BRACE?

The FDA product code for BONNER BRACE is IQK.

Related Clinical Trials

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Related Devices (Code: IQK)

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.

K930730DORMIE NECK SUPPORT SYSTEMThe Western Diagnostics Co.K926291SCHUL-TEC IMMOBILIZERMedical Emergency Support EquipmentK895477NOVA PILLOWNova Health Systems, Inc.K896042MEDICAL DISPOSABLE BEDDINGKeystone Veterinary Supplies, Inc.K882264BATTLE CREEK PILLOWBattle Creek Equipment Co.K850465CERVICAL COLLARS & HEAD HALTERSAbco Dealers, 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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