'EXMOOR' CAWOOD NASAL SPLINTS
K-Number: K864932 · 1987-03-04
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Device Summary
Frequently Asked Questions
What is the 'EXMOOR' CAWOOD NASAL SPLINTS?
'EXMOOR' CAWOOD NASAL SPLINTS is a medical device that received FDA 510(k) clearance on 1987-03-04. The listed applicant is Exmoor Plastics , Ltd.. The 510(k) number is K864932.
When did 'EXMOOR' CAWOOD NASAL SPLINTS receive FDA 510(k) clearance?
'EXMOOR' CAWOOD NASAL SPLINTS received FDA 510(k) clearance on 1987-03-04, under 510(k) number K864932.
Who is the listed applicant for 'EXMOOR' CAWOOD NASAL SPLINTS?
The FDA 510(k) record lists Exmoor Plastics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 'EXMOOR' CAWOOD NASAL SPLINTS?
The FDA product code for 'EXMOOR' CAWOOD NASAL SPLINTS is EPP.
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 Exmoor Plastics , 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: EPP)
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.
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