Atlas FDA

CAP-AID (IMPROVED)

FDA 510(k) clearance K964580 · decided 1997-01-10

Clearance details

K-number
K964580
Device name
CAP-AID (IMPROVED)
Applicant
Nebel, Inc.
Decision
Substantially Equivalent
Date received
1996-11-15
Decision date
1997-01-10
Days to decision
56 days
Clearance type
Traditional
Product code
FHA
Device class
1
Regulation number
876.5160
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Worcester, MA, 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
C3 EXTERNAL MALE BLADDER CONTROL DEVICE (K974040)Timm Research Co.1998-07-14
UROMED ALTERNATIVE BLADDER CONTROL CONTINENCE DEVICE(ABCPN-0026) (K971992)Uromed Corp.1997-08-01
MENTOR UROLOGY TRIPLE RIB OCCLUSION WRAP FOR MALE INCONTINENCE (K970308)Mentor Urology, Inc.1997-04-02
U-TEX (K955810)Laborie Medical Technologies, Ltd.1996-01-24
CAP-AID (K954959)Nebl, Inc.1995-12-06
THE ASSISTANT (K952841)Apple Medical Corp.1995-08-18
WILLIAMS PENILE ANESTHETIC RETAINER (K896160)Cook Urological, Inc.1990-02-16
DACOMED EXTERNAL MALE CONTINENCE DEVICE (K885323)Dacomed Corp.1989-02-08
COOK-VPI CONTINENCE CUFF (K863227)Cook Urological, Inc.1987-02-03
CLAMP, INCONTINENCE, BAUMRUCKER (K780137)Greenwald Surgical Co., Inc.1978-04-28

Recalls involving this device

No recalls on record reference this clearance.