HOBBS MEDICAL GRASPING FORCEPS— 510(k) K833125

Name: FDA 510(k) clearance K833125
Creator: U.S. Food and Drug Administration
Published: 1983-10-31

Substantially Equivalent

Hobbs Medical, Inc.

FDA 510(k) clearance K833125 for HOBBS MEDICAL GRASPING FORCEPS, Substantially Equivalent on 1983-10-31. 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: 1983-09-13
Decision date: 1983-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K030765 — HOBBS MISTIFIER SPRAY CATHETER2003-06-09
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Recalls naming K833125

K-number listed on FDA's recall record

Z-0034-2023 — Hobbs Medical Grasping Forceps Catalog Number:5004Class II·Ongoing·Hobbs Medical, Inc.·20220729
Z-0035-2023 — Hobbs Medical Grasping Forceps Catalog Number: 5008Class II·Ongoing·Hobbs Medical, Inc.·20220729
Z-0036-2023 — Hobbs Retrieval Forceps Catalog Number: 5018Class II·Ongoing·Hobbs Medical, Inc.·20220729

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K833125.

Data sourced from openFDA. This site is unofficial and independent of the FDA.