Visi - Stick Ophthalmic Suture Retainer Tape

FDA 510(k) K902010 · Visitec Co.

Substantially Equivalent

510(k) numberK902010

Submission

Device name
Visi - Stick Ophthalmic Suture Retainer Tape
Applicant
Visitec Co.
Sarasota, FL, US
Received
May 3, 1990
Decision date
June 20, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KGX – Tape And Bandage, Adhesive
Device class
Class I (low risk)
Regulation
21 CFR 880.5240
Specialty
General Hospital

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K933872Visi-Spear Eye SpongeHOZ · Traditional 12/27/1993SE
K923972Ophthalmic Fluid Distribution SetsFPK · Traditional 11/04/1992SE
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Questions and answers

When was Visi - Stick Ophthalmic Suture Retainer Tape cleared by the FDA?

Visi - Stick Ophthalmic Suture Retainer Tape (K902010) received a 510(k) decision of Substantially Equivalent on June 20, 1990, 48 days after the submission was received.

What is the product code of K902010?

The FDA product code is KGX – Tape And Bandage, Adhesive, a Class I (low risk) device regulated under 21 CFR 880.5240.