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FDA 510(k)

HOBBS MISTIFIER SPRAY CATHETER

K-Number: K030765 · 2003-06-09

ApplicantHobbs Medical, Inc.
Decision Date2003-06-09
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOBBS MISTIFIER SPRAY 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 2003-06-09 under 510(k) number K030765. 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 MISTIFIER SPRAY CATHETER?

HOBBS MISTIFIER SPRAY CATHETER is a medical device that received FDA 510(k) clearance on 2003-06-09. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K030765.

When did HOBBS MISTIFIER SPRAY CATHETER receive FDA 510(k) clearance?

HOBBS MISTIFIER SPRAY CATHETER received FDA 510(k) clearance on 2003-06-09, under 510(k) number K030765.

Who is the listed applicant for HOBBS MISTIFIER SPRAY 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 MISTIFIER SPRAY CATHETER?

The FDA product code for HOBBS MISTIFIER SPRAY CATHETER is OCX.

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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-UK933354HOBBS MEDICAL CLEANING BRUSHK922396FUJINON FORCEPS -- MODIFICATIONK921026PRESSURE GAUGE

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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.

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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.

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