LAKE WOUND CARE/TREATMENT KIT
K-Number: K873973 · 1987-11-20
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Device Summary
Frequently Asked Questions
What is the LAKE WOUND CARE/TREATMENT KIT?
LAKE WOUND CARE/TREATMENT KIT is a medical device that received FDA 510(k) clearance on 1987-11-20. The listed applicant is Lake Medical Products, Inc.. The 510(k) number is K873973.
When did LAKE WOUND CARE/TREATMENT KIT receive FDA 510(k) clearance?
LAKE WOUND CARE/TREATMENT KIT received FDA 510(k) clearance on 1987-11-20, under 510(k) number K873973.
Who is the listed applicant for LAKE WOUND CARE/TREATMENT KIT?
The FDA 510(k) record lists Lake Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAKE WOUND CARE/TREATMENT KIT?
The FDA product code for LAKE WOUND CARE/TREATMENT KIT is LRO.
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 Lake Medical Products, 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: LRO)
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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