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FDA 510(k)

MEHTA BRONCHIAL BIOSPY DRILL

K-Number: K954693 · 1995-10-23

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1995-10-23
Product CodeFCK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEHTA BRONCHIAL BIOSPY DRILL is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1995-10-23 under 510(k) number K954693. The device is classified under product code FCK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEHTA BRONCHIAL BIOSPY DRILL?

MEHTA BRONCHIAL BIOSPY DRILL is a medical device that received FDA 510(k) clearance on 1995-10-23. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K954693.

When did MEHTA BRONCHIAL BIOSPY DRILL receive FDA 510(k) clearance?

MEHTA BRONCHIAL BIOSPY DRILL received FDA 510(k) clearance on 1995-10-23, under 510(k) number K954693.

Who is the listed applicant for MEHTA BRONCHIAL BIOSPY DRILL?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEHTA BRONCHIAL BIOSPY DRILL?

The FDA product code for MEHTA BRONCHIAL BIOSPY DRILL is FCK.

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Related Devices (Code: FCK)

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.

K153763Howell Biliary Aspiration NeedleWilson-Cook Medical, Inc.K103326MULTIPLE BIOPSY SYSTEMUnited States Endoscopy Group, Inc.K062159RB12 SUCTION RECTAL BIOPSY SYSTEMAus Systems Pty , Ltd.K061201DSNARE DIMINUTIVE POLYPECTOMY AND SUCTION SYSTEM, MODEL 00711087United States Endoscopy Group, Inc.K051637DSNARE, MODEL 00711087United States Endoscopy Group, Inc.K944252BIOPSY DEVICE ACCESSORYBiopsys Medical, Inc.

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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