KIT, PREP, INSPIRON IV
K-Number: K760313 · 1976-08-04
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Device Summary
Frequently Asked Questions
What is the KIT, PREP, INSPIRON IV?
KIT, PREP, INSPIRON IV is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is Inspiron Corp.. The 510(k) number is K760313.
When did KIT, PREP, INSPIRON IV receive FDA 510(k) clearance?
KIT, PREP, INSPIRON IV received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760313.
Who is the listed applicant for KIT, PREP, INSPIRON IV?
The FDA 510(k) record lists Inspiron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KIT, PREP, INSPIRON IV?
The FDA product code for KIT, PREP, INSPIRON IV is KZD.
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 Inspiron Corp. 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: KZD)
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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