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FDA 510(k)

BASHAW CERVICAL IMMOBILIZER DEVICE

K-Number: K800108 · 1980-02-29

Decision Date1980-02-29
Product CodeIQK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BASHAW CERVICAL IMMOBILIZER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Bashaw Custom Specialties, Inc.. It received FDA 510(k) clearance on 1980-02-29 under 510(k) number K800108. 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 BASHAW CERVICAL IMMOBILIZER DEVICE?

BASHAW CERVICAL IMMOBILIZER DEVICE is a medical device that received FDA 510(k) clearance on 1980-02-29. The listed applicant is Bashaw Custom Specialties, Inc.. The 510(k) number is K800108.

When did BASHAW CERVICAL IMMOBILIZER DEVICE receive FDA 510(k) clearance?

BASHAW CERVICAL IMMOBILIZER DEVICE received FDA 510(k) clearance on 1980-02-29, under 510(k) number K800108.

Who is the listed applicant for BASHAW CERVICAL IMMOBILIZER DEVICE?

The FDA 510(k) record lists Bashaw Custom Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BASHAW CERVICAL IMMOBILIZER DEVICE?

The FDA product code for BASHAW CERVICAL IMMOBILIZER DEVICE is IQK.

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.

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.

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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