Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

POS-T-VAC (AVP-1000)

K-Number: K983245 · 1998-11-02

ApplicantPos-T-Vac, Inc.
Decision Date1998-11-02
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

POS-T-VAC (AVP-1000) is the device name listed in this FDA 510(k) record. The listed applicant is Pos-T-Vac, Inc.. It received FDA 510(k) clearance on 1998-11-02 under 510(k) number K983245. The device is classified under product code LKY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POS-T-VAC (AVP-1000)?

POS-T-VAC (AVP-1000) is a medical device that received FDA 510(k) clearance on 1998-11-02. The listed applicant is Pos-T-Vac, Inc.. The 510(k) number is K983245.

When did POS-T-VAC (AVP-1000) receive FDA 510(k) clearance?

POS-T-VAC (AVP-1000) received FDA 510(k) clearance on 1998-11-02, under 510(k) number K983245.

Who is the listed applicant for POS-T-VAC (AVP-1000)?

The FDA 510(k) record lists Pos-T-Vac, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POS-T-VAC (AVP-1000)?

The FDA product code for POS-T-VAC (AVP-1000) is LKY.

Other records listing Pos-T-Vac, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K020154VT-1K020258SUPPORT SLEEVEK012672BOSS-2000-2 VACUUM ERECTION DEVICEK012670BOSS 2000-3 VACUUM ERECTION DEVICEK983246POS-T-VAC (IVP-600)K981180REJOYN CONSTRICTION RING KIT, POS-T-VAC B-100 RING KIT, POS-T-VAC B-25 RING KIT AND POS-T-VAC B-10 RING KIT

View all 12 devices →

Related Devices (Code: LKY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K041573NANMA VACUUM PUMP PROXZEK MODEL 2M9498SNanma Mfg Co., Ltd.K032776VACURECT VACUUM CONSTRICTION DEVICEVacurect Manufacturing (Pty) , Ltd.K030119NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.K030913NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013113MODIFICATION TO NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013051NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑