KENDALL CURITY IODOFORM PACKING STRIP
K-Number: K973763 · 1997-12-31
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Device Summary
Frequently Asked Questions
What is the KENDALL CURITY IODOFORM PACKING STRIP?
KENDALL CURITY IODOFORM PACKING STRIP is a medical device that received FDA 510(k) clearance on 1997-12-31. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K973763.
When did KENDALL CURITY IODOFORM PACKING STRIP receive FDA 510(k) clearance?
KENDALL CURITY IODOFORM PACKING STRIP received FDA 510(k) clearance on 1997-12-31, under 510(k) number K973763.
Who is the listed applicant for KENDALL CURITY IODOFORM PACKING STRIP?
The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KENDALL CURITY IODOFORM PACKING STRIP?
The FDA product code for KENDALL CURITY IODOFORM PACKING STRIP is EFQ.
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 Kendall Healthcare Products Co. Div.Of Tyco Health 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: EFQ)
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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