CONFORMA(TM) PLASTER BANDAGES
K-Number: K873111 · 1987-10-09
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Device Summary
Frequently Asked Questions
What is the CONFORMA(TM) PLASTER BANDAGES?
CONFORMA(TM) PLASTER BANDAGES is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is The Kendal Co.. The 510(k) number is K873111.
When did CONFORMA(TM) PLASTER BANDAGES receive FDA 510(k) clearance?
CONFORMA(TM) PLASTER BANDAGES received FDA 510(k) clearance on 1987-10-09, under 510(k) number K873111.
Who is the listed applicant for CONFORMA(TM) PLASTER BANDAGES?
The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONFORMA(TM) PLASTER BANDAGES?
The FDA product code for CONFORMA(TM) PLASTER BANDAGES is ITG.
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 The Kendal Co. 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: ITG)
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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