JACOB CHUCK— 510(k) K802694
Substantially EquivalentRichard Wolf Medical Instruments Corp.
FDA 510(k) clearance K802694 for JACOB CHUCK, Substantially Equivalent on 1980-11-12. Applicant: Richard Wolf Medical Instruments Corp.. Device class: 1.
Clearance details
- Applicant
- Richard Wolf Medical Instruments Corp.
- Product code
- Code LXH
- Device class
- Class 1
- Regulation
- 21 CFR 888.4540
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code LXH
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
Adverse events under product code LXH
product code LXH- Death
- 11
- Injury
- 2,218
- Malfunction
- 31,318
- Total
- 33,547
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.