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FDA 510(k)

3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS

K-Number: K946024 · 1995-02-08

Applicant3M Healthcare
Decision Date1995-02-08
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS is the device name listed in this FDA 510(k) record. The listed applicant is 3M Healthcare. It received FDA 510(k) clearance on 1995-02-08 under 510(k) number K946024. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS?

3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS is a medical device that received FDA 510(k) clearance on 1995-02-08. The listed applicant is 3M Healthcare. The 510(k) number is K946024.

When did 3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS receive FDA 510(k) clearance?

3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS received FDA 510(k) clearance on 1995-02-08, under 510(k) number K946024.

Who is the listed applicant for 3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS?

The FDA 510(k) record lists 3M Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS?

The FDA product code for 3M PEDIATRIC LAPAROTOMY SHEET #7938/ #7938NS is KKX.

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Related Devices (Code: KKX)

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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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