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FDA 510(k)

DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN

K-Number: K901439 · 1990-06-11

ApplicantTelemed Systems, Inc.
Decision Date1990-06-11
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN is the device name listed in this FDA 510(k) record. The listed applicant is Telemed Systems, Inc.. It received FDA 510(k) clearance on 1990-06-11 under 510(k) number K901439. 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 DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN?

DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN is a medical device that received FDA 510(k) clearance on 1990-06-11. The listed applicant is Telemed Systems, Inc.. The 510(k) number is K901439.

When did DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN receive FDA 510(k) clearance?

DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN received FDA 510(k) clearance on 1990-06-11, under 510(k) number K901439.

Who is the listed applicant for DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN?

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

What is the FDA product code for DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN?

The FDA product code for DISP. ENDOSCOPE CLEANING BRUSH - SQUEEKY CLEAN is FEB.

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Other records listing Telemed Systems, Inc. as applicant

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K020379PPD BALLOON DILATATION CATHETERK013737MODIFICATION TO: 3-LUMEN DURALON OCCLUSION BALLOONK010412FLEXIBLE ENDOSCOPIC SCISSORSK9924025.0 FRENCH X 200CM X 35MM TIP TAPER-20MM CUTTING WIRE, 5.0 FRENCH X 200CM X 35MM TIP TAPER-30MM CUTTING WIRE, 5.0 FRENCHK992390HOT BIOPSY FORCEPS FEENESTRATED 230 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATED 160 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATDK974312REUSABLE BIOPSY FORCEPS OVAL CUP, REUSABLE BIOSY FORCEPS OVAL CUP W/NEEDLE, REUSABLE BIOPSY FORCEPS SERRATED CUP, REUSAR

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Related Devices (Code: FEB)

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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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