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FDA 510(k)

LOUNGE, TILT-A-BODY STRETCH

K-Number: K790572 · 1979-04-10

ApplicantInnovative Products, Inc.
Decision Date1979-04-10
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LOUNGE, TILT-A-BODY STRETCH is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Products, Inc.. It received FDA 510(k) clearance on 1979-04-10 under 510(k) number K790572. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOUNGE, TILT-A-BODY STRETCH?

LOUNGE, TILT-A-BODY STRETCH is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Innovative Products, Inc.. The 510(k) number is K790572.

When did LOUNGE, TILT-A-BODY STRETCH receive FDA 510(k) clearance?

LOUNGE, TILT-A-BODY STRETCH received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790572.

Who is the listed applicant for LOUNGE, TILT-A-BODY STRETCH?

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

What is the FDA product code for LOUNGE, TILT-A-BODY STRETCH?

The FDA product code for LOUNGE, TILT-A-BODY STRETCH is ION.

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Other records listing Innovative Products, 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.

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Related Devices (Code: ION)

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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