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FDA 510(k)

BIOPSY TRAY

K-Number: K941645 · 1994-07-14

Decision Date1994-07-14
Product CodeFRG
Advisory CommitteeHO
DecisionUnknown

Device Summary

BIOPSY TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Cush Medical Products. It received FDA 510(k) clearance on 1994-07-14 under 510(k) number K941645. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BIOPSY TRAY?

BIOPSY TRAY is a medical device that received FDA 510(k) clearance on 1994-07-14. The listed applicant is Cush Medical Products. The 510(k) number is K941645.

When did BIOPSY TRAY receive FDA 510(k) clearance?

BIOPSY TRAY received FDA 510(k) clearance on 1994-07-14, under 510(k) number K941645.

Who is the listed applicant for BIOPSY TRAY?

The FDA 510(k) record lists Cush Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOPSY TRAY?

The FDA product code for BIOPSY TRAY 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 Cush Medical Products 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 23 devices →

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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