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FDA 510(k)

CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE

K-Number: K960921 · 1996-04-17

Decision Date1996-04-17
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE is the device name listed in this FDA 510(k) record. The listed applicant is Codan Medlon, Inc.. It received FDA 510(k) clearance on 1996-04-17 under 510(k) number K960921. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE?

CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE is a medical device that received FDA 510(k) clearance on 1996-04-17. The listed applicant is Codan Medlon, Inc.. The 510(k) number is K960921.

When did CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE receive FDA 510(k) clearance?

CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE received FDA 510(k) clearance on 1996-04-17, under 510(k) number K960921.

Who is the listed applicant for CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE?

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

What is the FDA product code for CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE?

The FDA product code for CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE is LHI.

Related Clinical Trials

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.

Other records listing Codan Medlon, 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.

Related Devices (Code: LHI)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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