MODIFIED LABELING FOR POLYDERM WBC(TM)
K-Number: K890940 · 1989-04-17
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Device Summary
Frequently Asked Questions
What is the MODIFIED LABELING FOR POLYDERM WBC(TM)?
MODIFIED LABELING FOR POLYDERM WBC(TM) is a medical device that received FDA 510(k) clearance on 1989-04-17. The listed applicant is Laivan Corp.. The 510(k) number is K890940.
When did MODIFIED LABELING FOR POLYDERM WBC(TM) receive FDA 510(k) clearance?
MODIFIED LABELING FOR POLYDERM WBC(TM) received FDA 510(k) clearance on 1989-04-17, under 510(k) number K890940.
Who is the listed applicant for MODIFIED LABELING FOR POLYDERM WBC(TM)?
The FDA 510(k) record lists Laivan Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED LABELING FOR POLYDERM WBC(TM)?
The FDA product code for MODIFIED LABELING FOR POLYDERM WBC(TM) is NAD.
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 Laivan Corp. 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: NAD)
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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