13-320,13-330 Two Types Nazal Scissors-Heyman,Beck
FDA 510(k) K851763 · Artiberia
510(k) numberK851763
Submission
- Device name
- 13-320,13-330 Two Types Nazal Scissors-Heyman,Beck
- Applicant
- Artiberia
San Antonio, TX, US - Received
- April 25, 1985
- Decision date
- June 11, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KBD – Scissors, Nasal
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4420
- Specialty
- Ear, Nose, Throat
Other 510(k)s with product code KBD
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| K851726 | 1760/1 to 2010/34 Various Dental Filling InstrumenEIY · Traditional | 07/02/1985SE |
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| K851723 | 1300/10 to 1305/89-92 Various Cutting InstrumentsEKD · Traditional | 07/02/1985SE |
| K851722 | 1285/5 to 1295 Various Types of Dental ExcavatorsEKC · Traditional | 07/02/1985SE |
| K851721 | 1200/1 to 1240/15 Various Types of Dental ScalersEMN · Traditional | 07/02/1985SE |
Questions and answers
When was 13-320,13-330 Two Types Nazal Scissors-Heyman,Beck cleared by the FDA?
13-320,13-330 Two Types Nazal Scissors-Heyman,Beck (K851763) received a 510(k) decision of Substantially Equivalent on June 11, 1985, 47 days after the submission was received.
What is the product code of K851763?
The FDA product code is KBD – Scissors, Nasal, a Class I (low risk) device regulated under 21 CFR 874.4420.