INSPIREASE(R), DRUG DELIVERY SYSTEM
K-Number: K873793 · 1987-10-13
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Device Summary
Frequently Asked Questions
What is the INSPIREASE(R), DRUG DELIVERY SYSTEM?
INSPIREASE(R), DRUG DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1987-10-13. The listed applicant is Key Pharmaceuticals, Inc.. The 510(k) number is K873793.
When did INSPIREASE(R), DRUG DELIVERY SYSTEM receive FDA 510(k) clearance?
INSPIREASE(R), DRUG DELIVERY SYSTEM received FDA 510(k) clearance on 1987-10-13, under 510(k) number K873793.
Who is the listed applicant for INSPIREASE(R), DRUG DELIVERY SYSTEM?
The FDA 510(k) record lists Key Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INSPIREASE(R), DRUG DELIVERY SYSTEM?
The FDA product code for INSPIREASE(R), DRUG DELIVERY SYSTEM is CCQ.
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 Key Pharmaceuticals, 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: CCQ)
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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