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FDA 510(k)

BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET

K-Number: K884129 · 1988-12-21

ApplicantBio Medicus, Inc.
Decision Date1988-12-21
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET is the device name listed in this FDA 510(k) record. The listed applicant is Bio Medicus, Inc.. It received FDA 510(k) clearance on 1988-12-21 under 510(k) number K884129. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET?

BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET is a medical device that received FDA 510(k) clearance on 1988-12-21. The listed applicant is Bio Medicus, Inc.. The 510(k) number is K884129.

When did BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET receive FDA 510(k) clearance?

BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET received FDA 510(k) clearance on 1988-12-21, under 510(k) number K884129.

Who is the listed applicant for BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET?

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

What is the FDA product code for BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET?

The FDA product code for BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET is DQY.

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Other records listing Bio Medicus, 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.

K920761URINE CULTUR STABILIZATION TRANSPORT TUBEK903410BIO-MEDICUS CANNULA INTRODUCERK901253(PBS) PORTABLE BYPASS SYSTEM, MODEL 1000K901584BIO-MEDICUS BIO CONSOLE MODELS 540 A B CK894980BIO-CAL 370 HEATER/COOLERK883956BIO-MEDICUS TUBING CONNECTORS

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Related Devices (Code: DQY)

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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