Alligator Forecpts, Cupped Forceps
FDA 510(k) K791121 · Xomed, Inc.
510(k) numberK791121
Submission
- Device name
- Alligator Forecpts, Cupped Forceps
- Applicant
- Xomed, Inc.
Arnold, MO, US - Received
- June 15, 1979
- Decision date
- June 27, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JYR – Nipper, Malleus
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4420
- Specialty
- Ear, Nose, Throat
Other 510(k)s with product code JYR
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|---|---|---|---|
| K822170 | Incus NippersJYR · Traditional | Kelleher Corp. | 08/24/1982SE |
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Questions and answers
When was Alligator Forecpts, Cupped Forceps cleared by the FDA?
Alligator Forecpts, Cupped Forceps (K791121) received a 510(k) decision of Substantially Equivalent on June 27, 1979, 12 days after the submission was received.
What is the product code of K791121?
The FDA product code is JYR – Nipper, Malleus, a Class I (low risk) device regulated under 21 CFR 874.4420.