HOBBS MEDICAL RETRIEVAL BASKET— 510(k) K833124
Substantially EquivalentHobbs Medical, Inc.
FDA 510(k) clearance K833124 for HOBBS MEDICAL RETRIEVAL BASKET, Substantially Equivalent on 1983-11-29. 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
- Mchenry, IL, US
Recent devices under product code OCZ
view allMore clearances from Hobbs Medical, Inc.
view allRecalls naming K833124
K-number listed on FDA's recall record- Z-0026-2023 — Hobbs Helical Retrieval Basket Catalog Number: 4806
- Z-0027-2023 — Hobbs Helical Retrieval Basket Catalog Number: 4808
- Z-0028-2023 — Hobbs Helical Retrieval Basket Catalog Number: 4814
- Z-0029-2023 — Hobbs Helical Retrieval Basket Catalog Number: 4816
- Z-0030-2023 — Hobbs Helical Retrieval Basket Catalog Number: 4822
- Z-0031-2023 — Hobbs Helical Retrieval Basket Catalog Number: 4824
- Z-0033-2023 — Hobbs Helical Retrieval Basket Catalog Number: 4832
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K833124.
Data sourced from openFDA. This site is unofficial and independent of the FDA.