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FDA 510(k)

EXMOOR SUCTION CLEARANCE KIT

K-Number: K990366 · 1999-03-05

ApplicantExmoor Plastics , Ltd.
Decision Date1999-03-05
Product CodeLRC
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EXMOOR SUCTION CLEARANCE KIT 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 1999-03-05 under 510(k) number K990366. 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 SUCTION CLEARANCE KIT?

EXMOOR SUCTION CLEARANCE KIT is a medical device that received FDA 510(k) clearance on 1999-03-05. The listed applicant is Exmoor Plastics , Ltd.. The 510(k) number is K990366.

When did EXMOOR SUCTION CLEARANCE KIT receive FDA 510(k) clearance?

EXMOOR SUCTION CLEARANCE KIT received FDA 510(k) clearance on 1999-03-05, under 510(k) number K990366.

Who is the listed applicant for EXMOOR SUCTION CLEARANCE KIT?

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 SUCTION CLEARANCE KIT?

The FDA product code for EXMOOR SUCTION CLEARANCE KIT 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.

K093863EPIDRUMK980828EXMOOR MYRINGOTOMY KITK981143DILKES LASER/SUCTION CANNULAEK972700EXMOOR ATTIC AND MASTOID ANTRUM MIDDLE EAR IMPLANT (EMMETT CAMPBELL MD FACS PATTERN)K981088MILLS COLUMELLA PROSTHESISK981045EXMOOR TEFLON LOOP REPLACEMENT PROSTHESIS

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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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