← Product Code [LKY](/submissions/GU/subpart-f%E2%80%94therapeutic-devices/LKY) · K864833

# POS-T-VAC (K864833)

_Ekc, Inc. · LKY · Apr 10, 1987 · Gastroenterology, Urology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/LKY/K864833

## Device Facts

- **Applicant:** Ekc, Inc.
- **Product Code:** [LKY](/submissions/GU/subpart-f%E2%80%94therapeutic-devices/LKY.md)
- **Decision Date:** Apr 10, 1987
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 876.5020
- **Device Class:** Class 2
- **Review Panel:** Gastroenterology, Urology

## Regulatory 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.

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**Source:** [https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/LKY/K864833](https://fda.innolitics.com/submissions/GU/subpart-f%E2%80%94therapeutic-devices/LKY/K864833)

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