PRESSURE RELIEF SEAT CUSHION
K-Number: K842380 · 1984-06-28
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement