FDA 510(k)

MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY

K-Number: K854291 · 1985-11-26

Decision Date1985-11-26

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medsurg Industries, Inc.. It received FDA 510(k) clearance on 1985-11-26 under 510(k) number K854291. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY?

MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY is a medical device that received FDA 510(k) clearance on 1985-11-26. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K854291.

When did MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY receive FDA 510(k) clearance?

MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY received FDA 510(k) clearance on 1985-11-26, under 510(k) number K854291.

Who is the listed applicant for MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY?

The FDA 510(k) record lists Medsurg Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY?

The FDA product code for MED SURG PERCUTANEOUS ASPIRATION BIOPSY(PAB)TRAY is KNW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.