CODAN MEDLON BC110 VIAL ADAPTER CODAN SPIKE
K-Number: K960921 · 1996-04-17
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Device Summary
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
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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