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FDA 510(k)

VARI-SUPPORT LOW BACK POSTURE PILLOW

K-Number: K821838 · 1982-07-20

Decision Date1982-07-20
Product CodeCCX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VARI-SUPPORT 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 1982-07-20 under 510(k) number K821838. The device is classified under product code CCX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARI-SUPPORT LOW BACK POSTURE PILLOW?

VARI-SUPPORT LOW BACK POSTURE PILLOW is a medical device that received FDA 510(k) clearance on 1982-07-20. The listed applicant is Body Therapeutics, Inc.. The 510(k) number is K821838.

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

VARI-SUPPORT LOW BACK POSTURE PILLOW received FDA 510(k) clearance on 1982-07-20, under 510(k) number K821838.

Who is the listed applicant for VARI-SUPPORT 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 VARI-SUPPORT LOW BACK POSTURE PILLOW?

The FDA product code for VARI-SUPPORT LOW BACK POSTURE PILLOW is CCX.

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: CCX)

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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