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FDA 510(k)

BIOPSY KIT 781101, ASPIRATION

K-Number: K781830 · 1978-11-15

ApplicantVista Products, Inc.
Decision Date1978-11-15
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BIOPSY KIT 781101, ASPIRATION is the device name listed in this FDA 510(k) record. The listed applicant is Vista Products, Inc.. It received FDA 510(k) clearance on 1978-11-15 under 510(k) number K781830. The device is classified under product code HHK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPSY KIT 781101, ASPIRATION?

BIOPSY KIT 781101, ASPIRATION is a medical device that received FDA 510(k) clearance on 1978-11-15. The listed applicant is Vista Products, Inc.. The 510(k) number is K781830.

When did BIOPSY KIT 781101, ASPIRATION receive FDA 510(k) clearance?

BIOPSY KIT 781101, ASPIRATION received FDA 510(k) clearance on 1978-11-15, under 510(k) number K781830.

Who is the listed applicant for BIOPSY KIT 781101, ASPIRATION?

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

What is the FDA product code for BIOPSY KIT 781101, ASPIRATION?

The FDA product code for BIOPSY KIT 781101, ASPIRATION is HHK.

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Related Devices (Code: HHK)

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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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