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FDA 510(k)

PRESSURE RELIEF SEAT CUSHION

K-Number: K842380 · 1984-06-28

Decision Date1984-06-28
Product CodeKIC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PRESSURE RELIEF SEAT CUSHION is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1984-06-28 under 510(k) number K842380. 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 PRESSURE RELIEF SEAT CUSHION?

PRESSURE RELIEF SEAT CUSHION is a medical device that received FDA 510(k) clearance on 1984-06-28. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K842380.

When did PRESSURE RELIEF SEAT CUSHION receive FDA 510(k) clearance?

PRESSURE RELIEF SEAT CUSHION received FDA 510(k) clearance on 1984-06-28, under 510(k) number K842380.

Who is the listed applicant for PRESSURE RELIEF SEAT CUSHION?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRESSURE RELIEF SEAT CUSHION?

The FDA product code for PRESSURE RELIEF SEAT 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 American Pharmaseal Div. Ahsc 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.

View all 64 devices →

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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