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FDA 510(k)

SUNDERLAND NASAL TUBE

K-Number: K883668 · 1988-11-21

ApplicantExmoor Plastics , Ltd.
Decision Date1988-11-21
Product CodeBTQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SUNDERLAND NASAL 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 1988-11-21 under 510(k) number K883668. The device is classified under product code BTQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNDERLAND NASAL TUBE?

SUNDERLAND NASAL TUBE is a medical device that received FDA 510(k) clearance on 1988-11-21. The listed applicant is Exmoor Plastics , Ltd.. The 510(k) number is K883668.

When did SUNDERLAND NASAL TUBE receive FDA 510(k) clearance?

SUNDERLAND NASAL TUBE received FDA 510(k) clearance on 1988-11-21, under 510(k) number K883668.

Who is the listed applicant for SUNDERLAND NASAL 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 SUNDERLAND NASAL TUBE?

The FDA product code for SUNDERLAND NASAL TUBE is BTQ.

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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: BTQ)

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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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