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FDA 510(k)

'EXMOOR' SINGLE USE SUCTION TUBE

K-Number: K892504 · 1989-06-22

ApplicantExmoor Plastics , Ltd.
Decision Date1989-06-22
Product CodeLRC
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

'EXMOOR' SINGLE USE SUCTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Exmoor Plastics , Ltd.. It received FDA 510(k) clearance on 1989-06-22 under 510(k) number K892504. The device is classified under product code LRC. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 'EXMOOR' SINGLE USE SUCTION TUBE?

'EXMOOR' SINGLE USE SUCTION TUBE is a medical device that received FDA 510(k) clearance on 1989-06-22. The listed applicant is Exmoor Plastics , Ltd.. The 510(k) number is K892504.

When did 'EXMOOR' SINGLE USE SUCTION TUBE receive FDA 510(k) clearance?

'EXMOOR' SINGLE USE SUCTION TUBE received FDA 510(k) clearance on 1989-06-22, under 510(k) number K892504.

Who is the listed applicant for 'EXMOOR' SINGLE USE SUCTION TUBE?

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' SINGLE USE SUCTION TUBE?

The FDA product code for 'EXMOOR' SINGLE USE SUCTION TUBE is LRC.

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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.

K093863EPIDRUMK990366EXMOOR SUCTION CLEARANCE KITK980828EXMOOR MYRINGOTOMY KITK981143DILKES LASER/SUCTION CANNULAEK972700EXMOOR ATTIC AND MASTOID ANTRUM MIDDLE EAR IMPLANT (EMMETT CAMPBELL MD FACS PATTERN)K981088MILLS COLUMELLA PROSTHESIS

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Related Devices (Code: LRC)

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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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