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FDA 510(k)

MANAN UBK ULTRASONIC GUIDED BIOPSY KIT

K-Number: K852105 · 1985-06-18

ApplicantManan Manufacturing Co., Inc.
Decision Date1985-06-18
Product CodeFCH
Advisory CommitteeGU
DecisionUnknown

Device Summary

MANAN UBK ULTRASONIC GUIDED BIOPSY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Manan Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1985-06-18 under 510(k) number K852105. The device is classified under product code FCH. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MANAN UBK ULTRASONIC GUIDED BIOPSY KIT?

MANAN UBK ULTRASONIC GUIDED BIOPSY KIT is a medical device that received FDA 510(k) clearance on 1985-06-18. The listed applicant is Manan Manufacturing Co., Inc.. The 510(k) number is K852105.

When did MANAN UBK ULTRASONIC GUIDED BIOPSY KIT receive FDA 510(k) clearance?

MANAN UBK ULTRASONIC GUIDED BIOPSY KIT received FDA 510(k) clearance on 1985-06-18, under 510(k) number K852105.

Who is the listed applicant for MANAN UBK ULTRASONIC GUIDED BIOPSY KIT?

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

What is the FDA product code for MANAN UBK ULTRASONIC GUIDED BIOPSY KIT?

The FDA product code for MANAN UBK ULTRASONIC GUIDED BIOPSY KIT is FCH.

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Other records listing Manan Manufacturing Co., Inc. as applicant

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Related Devices (Code: FCH)

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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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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