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FDA 510(k)

LOW BACK POSTURE PILLOW

K-Number: K802442 · 1980-10-31

Decision Date1980-10-31
Product CodeIQK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LOW BACK POSTURE PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Body Therapeutics, Inc.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802442. 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 LOW BACK POSTURE PILLOW?

LOW BACK POSTURE PILLOW is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Body Therapeutics, Inc.. The 510(k) number is K802442.

When did LOW BACK POSTURE PILLOW receive FDA 510(k) clearance?

LOW BACK POSTURE PILLOW received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802442.

Who is the listed applicant for LOW BACK POSTURE PILLOW?

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

What is the FDA product code for LOW BACK POSTURE PILLOW?

The FDA product code for LOW BACK POSTURE 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 Body Therapeutics, 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

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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