HOBBS MEDICAL POLYPECTOMY SNARE— 510(k) K844074
Substantially EquivalentHobbs Medical, Inc.
FDA 510(k) clearance K844074 for HOBBS MEDICAL POLYPECTOMY SNARE, Substantially Equivalent on 1985-01-03. Applicant: Hobbs Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Hobbs Medical, Inc.
- Product code
- Code OCZ
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palmer, MA, US
Recent devices under product code OCZ
view allMore clearances from Hobbs Medical, Inc.
view allRecalls naming K844074
K-number listed on FDA's recall record- Z-0067-2023 — Hobbs Medical Polypectomy Snare Catalog Number: 7202
- Z-0068-2023 — Hobbs Medical Polypectomy Snare Catalog Number: 4563-OLY
- Z-0069-2023 — Hobbs Medical Polypectomy Snare Catalog Number: 4565-OLY
- Z-0070-2023 — Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY
- Z-1388-2022 — Hobbs Medical Polypectomy Snare, Catalog No. 7202
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K844074.
Data sourced from openFDA. This site is unofficial and independent of the FDA.