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FDA 510(k)

POS-T-VAC ID-300

K-Number: K961309 · 1996-06-10

ApplicantPos-T-Vac, Inc.
Decision Date1996-06-10
Product CodeKZH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POS-T-VAC ID-300 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 1996-06-10 under 510(k) number K961309. The device is classified under product code KZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POS-T-VAC ID-300?

POS-T-VAC ID-300 is a medical device that received FDA 510(k) clearance on 1996-06-10. The listed applicant is Pos-T-Vac, Inc.. The 510(k) number is K961309.

When did POS-T-VAC ID-300 receive FDA 510(k) clearance?

POS-T-VAC ID-300 received FDA 510(k) clearance on 1996-06-10, under 510(k) number K961309.

Who is the listed applicant for POS-T-VAC ID-300?

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 ID-300?

The FDA product code for POS-T-VAC ID-300 is KZH.

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 DEVICEK983245POS-T-VAC (AVP-1000)K983246POS-T-VAC (IVP-600)

View all 12 devices →

Related Devices (Code: KZH)

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.

K243232GripMateSynthon Hispania S.L.K213429AccuSert Needle InserterEmed Technologies CorporationK163400Orbit InserterYpsomed AGK160860MiniMed Quick-serterMedtronic MinimedK124026LOBSTER AUTO-INJECTORScandinavian Health LimitedK122837AUTOJECT 2 FOR GLASSY SYRINGEOwen Mumford, 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.

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