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FDA 510(k)

3M RAPIDSTAT LIGATING CLIP SYS

K-Number: K842382 · 1984-08-10

Applicant3M Company
Decision Date1984-08-10
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

3M RAPIDSTAT LIGATING CLIP SYS is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1984-08-10 under 510(k) number K842382. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M RAPIDSTAT LIGATING CLIP SYS?

3M RAPIDSTAT LIGATING CLIP SYS is a medical device that received FDA 510(k) clearance on 1984-08-10. The listed applicant is 3M Company. The 510(k) number is K842382.

When did 3M RAPIDSTAT LIGATING CLIP SYS receive FDA 510(k) clearance?

3M RAPIDSTAT LIGATING CLIP SYS received FDA 510(k) clearance on 1984-08-10, under 510(k) number K842382.

Who is the listed applicant for 3M RAPIDSTAT LIGATING CLIP SYS?

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 3M RAPIDSTAT LIGATING CLIP SYS?

The FDA product code for 3M RAPIDSTAT LIGATING CLIP SYS is FZP.

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.

View all 322 devices →

Related Devices (Code: FZP)

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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