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FDA 510(k)

STIFNICK IMMOBILIZING COLLAR

K-Number: K832990 · 1983-11-07

Decision Date1983-11-07
Product CodeIQK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STIFNICK IMMOBILIZING COLLAR is the device name listed in this FDA 510(k) record. The listed applicant is Laerdal California, Inc.. It received FDA 510(k) clearance on 1983-11-07 under 510(k) number K832990. 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 STIFNICK IMMOBILIZING COLLAR?

STIFNICK IMMOBILIZING COLLAR is a medical device that received FDA 510(k) clearance on 1983-11-07. The listed applicant is Laerdal California, Inc.. The 510(k) number is K832990.

When did STIFNICK IMMOBILIZING COLLAR receive FDA 510(k) clearance?

STIFNICK IMMOBILIZING COLLAR received FDA 510(k) clearance on 1983-11-07, under 510(k) number K832990.

Who is the listed applicant for STIFNICK IMMOBILIZING COLLAR?

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

What is the FDA product code for STIFNICK IMMOBILIZING COLLAR?

The FDA product code for STIFNICK IMMOBILIZING COLLAR 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.

Other records listing Laerdal California, 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.

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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