MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET
K-Number: K873109 · 1987-08-28
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Device Summary
Frequently Asked Questions
What is the MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET?
MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET is a medical device that received FDA 510(k) clearance on 1987-08-28. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K873109.
When did MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET receive FDA 510(k) clearance?
MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET received FDA 510(k) clearance on 1987-08-28, under 510(k) number K873109.
Who is the listed applicant for MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET?
The FDA 510(k) record lists Life-Tech Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET?
The FDA product code for MODEL CC-72 CAVERNOSOMETRY/CAVERNOSOGRAPHY SET is OJA.
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 Life-Tech Intl., 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.
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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