INOCULUM STDIZING SYS., INOCUPAC
K-Number: K781097 · 1978-08-14
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Device Summary
Frequently Asked Questions
What is the INOCULUM STDIZING SYS., INOCUPAC?
INOCULUM STDIZING SYS., INOCUPAC is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is 3M Company. The 510(k) number is K781097.
When did INOCULUM STDIZING SYS., INOCUPAC receive FDA 510(k) clearance?
INOCULUM STDIZING SYS., INOCUPAC received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781097.
Who is the listed applicant for INOCULUM STDIZING SYS., INOCUPAC?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
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 3M Company 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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