VACUUM ERECTION DEVICE (VED)

K901223 · Mission Pharmacal Co. · LKY · May 4, 1990 · Gastroenterology, Urology

Device Facts

Record IDK901223
Device NameVACUUM ERECTION DEVICE (VED)
ApplicantMission Pharmacal Co.
Product CodeLKY · Gastroenterology, Urology
Decision DateMay 4, 1990
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 876.5020
Device ClassClass 2

Regulatory Classification

Identification

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

Special Controls

*Classification.* Class II (special controls). The devices are exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9. The special control for these devices is the FDA guidance document entitled “Class II Special Controls Guidance Document: External Penile Rigidity Devices.” See § 876.1(e) for the availability of this guidance document.

Innolitics
510(k) Summary
Decision Summary
Classification Order
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