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FDA 510(k)

BATTLE CREEK PILLOW

K-Number: K882264 · 1988-08-09

Decision Date1988-08-09
Product CodeIQK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BATTLE CREEK PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Battle Creek Equipment Co.. It received FDA 510(k) clearance on 1988-08-09 under 510(k) number K882264. 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 BATTLE CREEK PILLOW?

BATTLE CREEK PILLOW is a medical device that received FDA 510(k) clearance on 1988-08-09. The listed applicant is Battle Creek Equipment Co.. The 510(k) number is K882264.

When did BATTLE CREEK PILLOW receive FDA 510(k) clearance?

BATTLE CREEK PILLOW received FDA 510(k) clearance on 1988-08-09, under 510(k) number K882264.

Who is the listed applicant for BATTLE CREEK PILLOW?

The FDA 510(k) record lists Battle Creek Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BATTLE CREEK PILLOW?

The FDA product code for BATTLE CREEK PILLOW 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 Battle Creek Equipment Co. 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 7 devices →

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

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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