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FDA 510(k)

'EXMOOR' ZOELLNER SUCKER ENDS

K-Number: K864937 · 1987-03-30

ApplicantExmoor Plastics , Ltd.
Decision Date1987-03-30
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

'EXMOOR' ZOELLNER SUCKER ENDS 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 1987-03-30 under 510(k) number K864937. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 'EXMOOR' ZOELLNER SUCKER ENDS?

'EXMOOR' ZOELLNER SUCKER ENDS is a medical device that received FDA 510(k) clearance on 1987-03-30. The listed applicant is Exmoor Plastics , Ltd.. The 510(k) number is K864937.

When did 'EXMOOR' ZOELLNER SUCKER ENDS receive FDA 510(k) clearance?

'EXMOOR' ZOELLNER SUCKER ENDS received FDA 510(k) clearance on 1987-03-30, under 510(k) number K864937.

Who is the listed applicant for 'EXMOOR' ZOELLNER SUCKER ENDS?

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' ZOELLNER SUCKER ENDS?

The FDA product code for 'EXMOOR' ZOELLNER SUCKER ENDS is JOL.

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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: JOL)

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.

K051370STERILE SALINE FOR DEVICE CARE, STERILE WATER FOR DEVICE CARE, MODELS 2F7121, 2F8014Baxter Healthcare CorpK000266PRIMARY CARE SOLUTIONS STERILE SALINE-0.9% SODIUM CHLORIDE FOR DEVICE IRRIGATIONPrimary Care Solutions, Inc.K000265PRIMARY CARE SOLUTIONS STERILE WATER DEVICE IRRIGATIONPrimary Care Solutions, Inc.K003402WELCON STERILE WATER FOR DEVICE IRRIGATION; WELCON STERILE 0.9% NORMAL SALINE FOR DEVICE IRRIGATIONWelcon, Inc.K994321STERILE WATER AND 0.9% SODIUM CHLORIDE FOR IRRIGATION, USPAutomatic Liquid Packaging, Inc.K974758HYDROX STERILE WATER 4 OZ. CUP 120 ML., HYDROX STERILE WATER 100 ML BOTTLEHydrox Laboratories

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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