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FDA 510(k)

MODIFICATION TO SKVEKPATCH

K-Number: K984177 · 1998-12-18

ApplicantMarine Polymer Technologies, Inc.
Decision Date1998-12-18
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

MODIFICATION TO SKVEKPATCH is the device name listed in this FDA 510(k) record. The listed applicant is Marine Polymer Technologies, Inc.. It received FDA 510(k) clearance on 1998-12-18 under 510(k) number K984177. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MODIFICATION TO SKVEKPATCH?

MODIFICATION TO SKVEKPATCH is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Marine Polymer Technologies, Inc.. The 510(k) number is K984177.

When did MODIFICATION TO SKVEKPATCH receive FDA 510(k) clearance?

MODIFICATION TO SKVEKPATCH received FDA 510(k) clearance on 1998-12-18, under 510(k) number K984177.

Who is the listed applicant for MODIFICATION TO SKVEKPATCH?

The FDA 510(k) record lists Marine Polymer Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO SKVEKPATCH?

The FDA product code for MODIFICATION TO SKVEKPATCH is KMF.

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Other records listing Marine Polymer Technologies, Inc. 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.

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Related Devices (Code: KMF)

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, Inc.

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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