Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HOBBS MEDICAL/JAYCO ASPIRATION CATHETER

K-Number: K844550 · 1985-01-03

ApplicantHobbs Medical, Inc.
Decision Date1985-01-03
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOBBS MEDICAL/JAYCO ASPIRATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Hobbs Medical, Inc.. It received FDA 510(k) clearance on 1985-01-03 under 510(k) number K844550. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOBBS MEDICAL/JAYCO ASPIRATION CATHETER?

HOBBS MEDICAL/JAYCO ASPIRATION CATHETER is a medical device that received FDA 510(k) clearance on 1985-01-03. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K844550.

When did HOBBS MEDICAL/JAYCO ASPIRATION CATHETER receive FDA 510(k) clearance?

HOBBS MEDICAL/JAYCO ASPIRATION CATHETER received FDA 510(k) clearance on 1985-01-03, under 510(k) number K844550.

Who is the listed applicant for HOBBS MEDICAL/JAYCO ASPIRATION CATHETER?

The FDA 510(k) record lists Hobbs Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOBBS MEDICAL/JAYCO ASPIRATION CATHETER?

The FDA product code for HOBBS MEDICAL/JAYCO ASPIRATION CATHETER is OCX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hobbs Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241874Aspiration Catheter (2189)K182927Pulmonary Cytology BrushK093079TOUCHSOFT COAGULATOR WITH BANANA FITTING, MODEL 4581 AND WITH UNIVERSAL FITTING, MODEL 4581-UK030765HOBBS MISTIFIER SPRAY CATHETERK933354HOBBS MEDICAL CLEANING BRUSHK922396FUJINON FORCEPS -- MODIFICATION

View all 21 devices →

Related Devices (Code: OCX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251986AUXILIARY WATER TUBE MAJ-855Olympus Medical Systems CorporationK251997Single-Use Biopsy Valve (MAJ-1555)Olympus Medical Systems CorporationK242586ArgoCap (200.52)Ovesco Endoscopy AGK241704Endoscopic Water PumpHangzhou AGS MedTech Co., Ltd.K242357Water Container (MAJ-901); Water Container (MAJ-902)Olympus Medical Systems CorporationK241874Aspiration Catheter (2189)Hobbs Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑