Atlas FDA

EXTENSION SETS

FDA 510(k) clearance K760385 · decided 1976-11-02

Clearance details

K-number
K760385
Device name
EXTENSION SETS
Applicant
B. Braun Instruments
Decision
Substantially Equivalent
Date received
1976-08-05
Decision date
1976-11-02
Days to decision
89 days
Clearance type
Traditional
Product code
KGZ
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
AART SILICONE TUBING (K022306)Aesthetic and Reconstructive Technologies, Inc.2002-10-10
BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBING (K974295)Byron Medical1998-02-10
WOUND DRAINAGE HOLDER (K973183)R & D Medical Products, Inc.1998-01-23
DURALASTIC SILICONE TUBING (K955433)Allied Biomedical Corp.1996-01-26
NAVARRE PERCUTANEOUS ACCESS SET (K942315)Navarre Biomedical , Ltd.1994-07-08
PALESTRANT IRRIGATION AND DRAINAGE SET (K896087)North American Instrument Corp.1989-11-03
OPTICAL CATHETER(TM) INTRODUCER SETS (K895041)Medical Dynamics, Inc.1989-10-16
DESERET PRN ADAPTER (K893406)Deseret Medical, Inc.1989-06-22
CONCEPT SWITCHING STICK (K873009)Concept, Inc.1987-08-17
HCI GENERAL PURPOSE CATHETER STYLET (K870014)Health Care Innovations, Inc.1987-02-06
TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SU (K864115)Cathaid, Inc.1986-11-07
ANGIO MED DISPOSABLE PRESSURE CONNECTORS (K855078)Angiomed U.S., Inc.1986-02-19

Recalls involving this device

No recalls on record reference this clearance.