POSTERIOR NASAL EPISTAXIS INSTRUMENTS— 510(k) K911756
Substantially EquivalentRichard Wolf Medical Instruments Corp.
FDA 510(k) clearance K911756 for POSTERIOR NASAL EPISTAXIS INSTRUMENTS, Substantially Equivalent on 1991-10-24. Applicant: Richard Wolf Medical Instruments Corp.. Device class: 1.
Clearance details
- Applicant
- Richard Wolf Medical Instruments Corp.
- Product code
- Code ECB
- Device class
- Class 1
- Regulation
- 21 CFR 872.4565
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rosemont, IL, US
Recent devices under product code ECB
view allMore clearances from Richard Wolf Medical Instruments Corp.
view all- K151282 — core nova Complete Operating Room Endoscopy
- K130423 — THE RICHARD WOLF ENDOCAM LOGIC HD CAMERA SYSTEM 5525
- K121724 — ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2
- K120898 — KEYPORT SYSTEM, INCLUDES: KEYPORT SILICONE SEALING INSERT 8850XXX KEYPORT TRUCAR 8850XX KEYPORT TROCAR 8850XX SEALING CA
- K090776 — MEGAPULSE LASER SYSTEM AND FIBERS
Data sourced from openFDA. This site is unofficial and independent of the FDA.