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FDA 510(k)

HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM

K-Number: K781038 · 1978-08-14

ApplicantQuinton, Inc.
Decision Date1978-08-14
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1978-08-14 under 510(k) number K781038. 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 HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM?

HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Quinton, Inc.. The 510(k) number is K781038.

When did HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM receive FDA 510(k) clearance?

HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781038.

Who is the listed applicant for HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM?

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

What is the FDA product code for HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM?

The FDA product code for HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM is KNW.

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Other records listing Quinton, Inc. as applicant

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Related Devices (Code: KNW)

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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