Talc Dispenser Syringe

FDA 510(k) K930610 · Nusurg, Inc.

Substantially Equivalent

510(k) numberK930610

Submission

Device name
Talc Dispenser Syringe
Applicant
Nusurg, Inc.
Cincinnati, OH, US
Received
February 5, 1993
Decision date
November 4, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KYZ – Syringe, Irrigating (Non Dental)
Device class
Class I (low risk)
Regulation
21 CFR 880.6960
Specialty
General Hospital

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Questions and answers

When was Talc Dispenser Syringe cleared by the FDA?

Talc Dispenser Syringe (K930610) received a 510(k) decision of Substantially Equivalent on November 4, 1993, 272 days after the submission was received.

What is the product code of K930610?

The FDA product code is KYZ – Syringe, Irrigating (Non Dental), a Class I (low risk) device regulated under 21 CFR 880.6960.