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FDA 510(k)

BVI SLING

K-Number: K002233 · 2000-10-13

ApplicantBio-Vascular, Inc.
Decision Date2000-10-13
Product CodePAJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BVI SLING is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Vascular, Inc.. It received FDA 510(k) clearance on 2000-10-13 under 510(k) number K002233. The device is classified under product code PAJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BVI SLING?

BVI SLING is a medical device that received FDA 510(k) clearance on 2000-10-13. The listed applicant is Bio-Vascular, Inc.. The 510(k) number is K002233.

When did BVI SLING receive FDA 510(k) clearance?

BVI SLING received FDA 510(k) clearance on 2000-10-13, under 510(k) number K002233.

Who is the listed applicant for BVI SLING?

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

What is the FDA product code for BVI SLING?

The FDA product code for BVI SLING is PAJ.

Related Clinical Trials

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Other records listing Bio-Vascular, 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.

K992537PERI-STRIPS-SLEEVE, PERI-STRIPS-STRIP AND PERI-STRIPS DRY (NON-NAOH-TREATED AND NAOH-TREATEDK983602CV PERI-GUARD AND VASCU-GUARDK983581OCU-GUARD AND OCU-GUARD SUPPLEK983162PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS - SLEEVE, PERI-STRIPS-STRIPS, PERI-STRIPS DRY, VASCK981624FLO-THRUK982282DURA-GUARD - DURAL REPAIR PATCH

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Related Devices (Code: PAJ)

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.

K051190XENFORM SOFT TISSUE REPAIR MATRIXTei Biosciences, Inc.

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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