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FDA 510(k)

MEDSURG PERCUTANEOUS ASPIRATION BIOPSY (PAB) TRAY

K-Number: K870892 · 1987-04-10

Decision Date1987-04-10
Product CodeFSM
Advisory CommitteeSU
DecisionUnknown

Device Summary

MEDSURG 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 1987-04-10 under 510(k) number K870892. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDSURG PERCUTANEOUS ASPIRATION BIOPSY (PAB) TRAY?

MEDSURG PERCUTANEOUS ASPIRATION BIOPSY (PAB) TRAY is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Medsurg Industries, Inc.. The 510(k) number is K870892.

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

MEDSURG PERCUTANEOUS ASPIRATION BIOPSY (PAB) TRAY received FDA 510(k) clearance on 1987-04-10, under 510(k) number K870892.

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

The FDA product code for MEDSURG PERCUTANEOUS ASPIRATION BIOPSY (PAB) TRAY is FSM.

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 Medsurg Industries, Inc. 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.

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Related Devices (Code: FSM)

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

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

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