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FDA 510(k)

JAY CUSHION

K-Number: K834517 · 1984-01-17

Decision Date1984-01-17
Product CodeKIC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JAY CUSHION is the device name listed in this FDA 510(k) record. The listed applicant is Jay Medical, Ltd.. It received FDA 510(k) clearance on 1984-01-17 under 510(k) number K834517. The device is classified under product code KIC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAY CUSHION?

JAY CUSHION is a medical device that received FDA 510(k) clearance on 1984-01-17. The listed applicant is Jay Medical, Ltd.. The 510(k) number is K834517.

When did JAY CUSHION receive FDA 510(k) clearance?

JAY CUSHION received FDA 510(k) clearance on 1984-01-17, under 510(k) number K834517.

Who is the listed applicant for JAY CUSHION?

The FDA 510(k) record lists Jay Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JAY CUSHION?

The FDA product code for JAY CUSHION is KIC.

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 Jay Medical, Ltd. 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: KIC)

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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