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510(k) K020969

VACURECT VACUUM CONSTRICTION DEVICE by Vacurect Manufacturing (Pty) , Ltd. — Product Code LKY

K020969 is an FDA 510(k) premarket notification submitted by Vacurect Manufacturing (Pty) , Ltd. for the device "VACURECT VACUUM CONSTRICTION DEVICE". The FDA issued a decision of Substantially Equivalent on June 5, 2002. The device falls under product code LKY (Device, External Penile Rigidity), a Class II device regulated under 21 CFR 876.5020. Vacurect Manufacturing (Pty) , Ltd. has at least 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 5, 2002
Date Received
March 26, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, External Penile Rigidity
Device Class
Class II
Regulation Number
876.5020
Review Panel
GU
Submission Type

Intended to create or maintain sufficient penile rigidity for sexual intercourse. These include vacuum pumps, constriction rings, and penile splints, which are mechanical, powered or pneumatic devices.

Other clearances by Vacurect Manufacturing (Pty) , Ltd.

  • K032776 — VACURECT VACUUM CONSTRICTION DEVICE (October 3, 2003)

Other clearances for product code LKY

  • K041573 — NANMA VACUUM PUMP PROXZEK MODEL 2M9498S (August 25, 2004)
  • K032776 — VACURECT VACUUM CONSTRICTION DEVICE (October 3, 2003)
  • K030119 — NANMA ADJUSTABLE CONSTRICTION RING (August 6, 2003)
  • K030913 — NANMA VACUUM PUMP (June 3, 2003)
  • K013113 — MODIFICATION TO NANMA VACUUM PUMP (December 20, 2002)
  • K013051 — NANMA ADJUSTABLE CONSTRICTION RING (August 22, 2002)
  • K013053 — MODIFICATION TO NANMA NON-ADJUSTABLE CONSTRICTION RING (May 9, 2002)
  • K020258 — SUPPORT SLEEVE (April 4, 2002)
  • K020154 — VT-1 (April 4, 2002)
  • K020082 — ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYS (February 5, 2002)

FDA data resources