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FDA 510(k)

SUPER SLICK

K-Number: K853882 · 1985-11-18

ApplicantTang Products
Decision Date1985-11-18
Product CodeKMT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUPER SLICK is the device name listed in this FDA 510(k) record. The listed applicant is Tang Products. It received FDA 510(k) clearance on 1985-11-18 under 510(k) number K853882. The device is classified under product code KMT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER SLICK?

SUPER SLICK is a medical device that received FDA 510(k) clearance on 1985-11-18. The listed applicant is Tang Products. The 510(k) number is K853882.

When did SUPER SLICK receive FDA 510(k) clearance?

SUPER SLICK received FDA 510(k) clearance on 1985-11-18, under 510(k) number K853882.

Who is the listed applicant for SUPER SLICK?

The FDA 510(k) record lists Tang Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPER SLICK?

The FDA product code for SUPER SLICK is KMT.

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Related Devices (Code: KMT)

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.

K031809PERIO PROTECT TRAYPerio Protect, LLCK904914DENTAL VACUUM INJECTION TRAYThe Lebanon Vac-Tray Corp.K871784TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLIColgate-Hoyt LaboratoriesK820104NUPRO* GEL TRAYJohnson & Johnson Professionals, Inc.K811154HOYT ECONO-TRAYHoyt LaboratoriesK780712KERR DISCOVERY DISPOSABLE FLUORIDE TRAYKerr Corporation (Danbury)

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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