TODD MEDICAL/SKILLED CARE PRODUCTS
K-Number: K873469 · 1987-10-29
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Device Summary
Frequently Asked Questions
What is the TODD MEDICAL/SKILLED CARE PRODUCTS?
TODD MEDICAL/SKILLED CARE PRODUCTS is a medical device that received FDA 510(k) clearance on 1987-10-29. The listed applicant is Todd Medical, Inc.. The 510(k) number is K873469.
When did TODD MEDICAL/SKILLED CARE PRODUCTS receive FDA 510(k) clearance?
TODD MEDICAL/SKILLED CARE PRODUCTS received FDA 510(k) clearance on 1987-10-29, under 510(k) number K873469.
Who is the listed applicant for TODD MEDICAL/SKILLED CARE PRODUCTS?
The FDA 510(k) record lists Todd Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TODD MEDICAL/SKILLED CARE PRODUCTS?
The FDA product code for TODD MEDICAL/SKILLED CARE PRODUCTS is LRP.
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 Todd Medical, 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: LRP)
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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