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FDA 510(k)

LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60

K-Number: K980091 · 1998-04-09

ApplicantCosmaceutical Marketing, Inc.
Decision Date1998-04-09
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60 is the device name listed in this FDA 510(k) record. The listed applicant is Cosmaceutical Marketing, Inc.. It received FDA 510(k) clearance on 1998-04-09 under 510(k) number K980091. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60?

LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60 is a medical device that received FDA 510(k) clearance on 1998-04-09. The listed applicant is Cosmaceutical Marketing, Inc.. The 510(k) number is K980091.

When did LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60 receive FDA 510(k) clearance?

LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60 received FDA 510(k) clearance on 1998-04-09, under 510(k) number K980091.

Who is the listed applicant for LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60?

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

What is the FDA product code for LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60?

The FDA product code for LUBRISCAN ULTRA SCAN GEL +, MODEL RG2-60 is ITX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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