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FDA 510(k)

ADVANCED DIAGNOSTIC VIEWER (ADV)

K-Number: K963697 · 1996-11-27

ApplicantBio-Vascular, Inc.
Decision Date1996-11-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANCED DIAGNOSTIC VIEWER (ADV) 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 1996-11-27 under 510(k) number K963697. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCED DIAGNOSTIC VIEWER (ADV)?

ADVANCED DIAGNOSTIC VIEWER (ADV) is a medical device that received FDA 510(k) clearance on 1996-11-27. The listed applicant is Bio-Vascular, Inc.. The 510(k) number is K963697.

When did ADVANCED DIAGNOSTIC VIEWER (ADV) receive FDA 510(k) clearance?

ADVANCED DIAGNOSTIC VIEWER (ADV) received FDA 510(k) clearance on 1996-11-27, under 510(k) number K963697.

Who is the listed applicant for ADVANCED DIAGNOSTIC VIEWER (ADV)?

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 ADVANCED DIAGNOSTIC VIEWER (ADV)?

The FDA product code for ADVANCED DIAGNOSTIC VIEWER (ADV) is LLZ.

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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.

K002233BVI SLINGK992537PERI-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-THRU

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Related Devices (Code: LLZ)

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.

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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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