Atlas FDA

FLAT DRAIN

FDA 510(k) clearance K813063 · decided 1981-12-18

Clearance details

K-number
K813063
Device name
FLAT DRAIN
Applicant
Sil-Med Corp.
Decision
Substantially Equivalent
Date received
1981-10-30
Decision date
1981-12-18
Days to decision
49 days
Clearance type
Traditional
Product code
GBW
Device class
1
Regulation number
878.4200
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
MINI-PORT (K992904)Taut, Inc.1999-10-05
INTRADUCER (K992907)Taut, Inc.1999-10-05
INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450 (K972112)Taut, Inc.1997-12-01
ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN (K961194)Sil-Med Corp.1996-08-08
MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER (K960426)Medical Components, Inc.1996-03-21
MEDIASTINAL SILICONE DRAINS (K942709)Sil-Med Corp.1996-01-04
ARGYLE TURKEL SAFETY TROCAR THORACIC CATHETER (K933510)Sherwood Medical Co.1994-02-24
BIFURCATED SUCTION/IRRIGAT TUBING SET W/PUSH BUTTO (K926477)Core Dynamics, Inc.1993-11-12
STERILE CHEST TUBE (K913733)Vascular Products, Inc.1991-10-08
HOUTS HYSTERECTOMY DRAIN (K894220)Helix Medical, Inc.1989-08-24
MADEGOM LTDA. PENROSE DRAIN TUBING (K894119)Madegom1989-08-18
NELSON-JUNG PLEURAL CATH (K854812)Research Medical, Inc.1986-02-11

Recalls involving this device

No recalls on record reference this clearance.