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FDA 510(k)

HOBBS MEDICAL CLEANING BRUSH

K-Number: K933354 · 1993-10-28

ApplicantHobbs Medical, Inc.
Decision Date1993-10-28
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOBBS MEDICAL CLEANING BRUSH 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 1993-10-28 under 510(k) number K933354. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOBBS MEDICAL CLEANING BRUSH?

HOBBS MEDICAL CLEANING BRUSH is a medical device that received FDA 510(k) clearance on 1993-10-28. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K933354.

When did HOBBS MEDICAL CLEANING BRUSH receive FDA 510(k) clearance?

HOBBS MEDICAL CLEANING BRUSH received FDA 510(k) clearance on 1993-10-28, under 510(k) number K933354.

Who is the listed applicant for HOBBS MEDICAL CLEANING BRUSH?

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 CLEANING BRUSH?

The FDA product code for HOBBS MEDICAL CLEANING BRUSH is FEB.

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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-UK030765HOBBS MISTIFIER SPRAY CATHETERK922396FUJINON FORCEPS -- MODIFICATIONK921026PRESSURE GAUGE

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Related Devices (Code: FEB)

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.

K241168System 83 Revolve Endoscope Washer/DisinfectorWassenburg Medical, Inc.K243433enspire 3000 Cleaning and Liquid Chemical Sterilant Processing SystemSTERIS CorporationK230930enspire 3000 Cleaning and Liquid Chemical Sterile Processing SystemSTERIS CorporationK213833SCOPE BUDDY PLUS Endoscope Flushing AidMedivators, Inc.K201920Endoscope Reprocessor OER-EliteOlympus Medical Systems Corp.K173590System 83 Plus Washer/DisinfectorCustom Ultrasonics, 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.

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