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FDA 510(k)

SENSOR PAD

K-Number: K973450 · 1997-11-14

Decision Date1997-11-14
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SENSOR PAD is the device name listed in this FDA 510(k) record. The listed applicant is Inventive Products, Inc.. It received FDA 510(k) clearance on 1997-11-14 under 510(k) number K973450. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSOR PAD?

SENSOR PAD is a medical device that received FDA 510(k) clearance on 1997-11-14. The listed applicant is Inventive Products, Inc.. The 510(k) number is K973450.

When did SENSOR PAD receive FDA 510(k) clearance?

SENSOR PAD received FDA 510(k) clearance on 1997-11-14, under 510(k) number K973450.

Who is the listed applicant for SENSOR PAD?

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

What is the FDA product code for SENSOR PAD?

The FDA product code for SENSOR PAD is IYO.

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 Inventive 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.

Related Devices (Code: IYO)

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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