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FDA 510(k)

CHIROPRACTIC MASSAGE PILLOW

K-Number: K896947 · 1990-01-02

ApplicantIntl. Pacific Industrial Corp. (Usa), Inc.
Decision Date1990-01-02
Product CodeIRO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CHIROPRACTIC MASSAGE PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Pacific Industrial Corp. (Usa), Inc.. It received FDA 510(k) clearance on 1990-01-02 under 510(k) number K896947. The device is classified under product code IRO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHIROPRACTIC MASSAGE PILLOW?

CHIROPRACTIC MASSAGE PILLOW is a medical device that received FDA 510(k) clearance on 1990-01-02. The listed applicant is Intl. Pacific Industrial Corp. (Usa), Inc.. The 510(k) number is K896947.

When did CHIROPRACTIC MASSAGE PILLOW receive FDA 510(k) clearance?

CHIROPRACTIC MASSAGE PILLOW received FDA 510(k) clearance on 1990-01-02, under 510(k) number K896947.

Who is the listed applicant for CHIROPRACTIC MASSAGE PILLOW?

The FDA 510(k) record lists Intl. Pacific Industrial Corp. (Usa), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHIROPRACTIC MASSAGE PILLOW?

The FDA product code for CHIROPRACTIC MASSAGE PILLOW is IRO.

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.

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Other records listing Intl. Pacific Industrial Corp. (Usa), 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.

K892485PATIENT EXAMINATION GLOVES (LATEX)

Related Devices (Code: IRO)

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.

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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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