FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HOUTS HYSTERECTOMY DRAIN

K Number: K894220 · Decision Aug 24, 1989
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
16
Applicant Total
14
Review Days
66

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Basic Information

Device Name
HOUTS HYSTERECTOMY DRAIN
K Number
K894220
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Helix Medical, Inc.
Date Received
June 19, 1989
Decision Date
August 24, 1989
Product Code
GBW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GBW Catheter, Peritoneal

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Other Clearances by Helix Medical, Inc.

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K945287 INHEALTH BLOM-SINGER INDWELLING VALVED INSERT ACCESSORY DEVICE
K945288 INHEALTH BLOM-SINGER INDWELLING PLUG INSERT ACCESSORY DEVICE
K932120 BLOM-SINGER INDWELLING LOW PRESSURE VOICE PROSTHES
K932163 BLOM-SINGER VOICE PROSTHESIS FLUSHING PIPET
K930105 BLOM-SINGER LOW PRESSURE VOICE PROSTHESIS,P.I.D.S.
K920090 BLOM-SINGER TRACHEOESOPHAGEAL PUNCTURE SET
K915786 BLOM-SINGER HUMID/FIL SYST INHEALTH IN-LINE HUMID.
K904729 BLOM-SINGER SHOWER GUARD
Search all 14 clearances from Helix Medical, Inc. →