STERI-LOK DUAL PURPOSE PACKAGING/8400
K-Number: K811670 · 1981-07-10
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Device Summary
Frequently Asked Questions
What is the STERI-LOK DUAL PURPOSE PACKAGING/8400?
STERI-LOK DUAL PURPOSE PACKAGING/8400 is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is 3M Company. The 510(k) number is K811670.
When did STERI-LOK DUAL PURPOSE PACKAGING/8400 receive FDA 510(k) clearance?
STERI-LOK DUAL PURPOSE PACKAGING/8400 received FDA 510(k) clearance on 1981-07-10, under 510(k) number K811670.
Who is the listed applicant for STERI-LOK DUAL PURPOSE PACKAGING/8400?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERI-LOK DUAL PURPOSE PACKAGING/8400?
The FDA product code for STERI-LOK DUAL PURPOSE PACKAGING/8400 is FRG.
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.
Related Devices (Code: FRG)
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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