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FDA 510(k)

POS-T-VAC (IVP-600)

K-Number: K983246 · 1998-11-02

Decision Date1998-11-02
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

POS-T-VAC (IVP-600) 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 K983246. 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 (IVP-600)?

POS-T-VAC (IVP-600) 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 K983246.

When did POS-T-VAC (IVP-600) receive FDA 510(k) clearance?

POS-T-VAC (IVP-600) received FDA 510(k) clearance on 1998-11-02, under 510(k) number K983246.

Who is the listed applicant for POS-T-VAC (IVP-600)?

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 (IVP-600)?

The FDA product code for POS-T-VAC (IVP-600) 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.

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.

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.

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