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FDA 510(k)

DAP II BIOPSY GUIDE

K-Number: K830999 · 1983-07-12

ApplicantRapid Machine & Tool Corp.
Decision Date1983-07-12
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DAP II BIOPSY GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Rapid Machine & Tool Corp.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K830999. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAP II BIOPSY GUIDE?

DAP II BIOPSY GUIDE is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Rapid Machine & Tool Corp.. The 510(k) number is K830999.

When did DAP II BIOPSY GUIDE receive FDA 510(k) clearance?

DAP II BIOPSY GUIDE received FDA 510(k) clearance on 1983-07-12, under 510(k) number K830999.

Who is the listed applicant for DAP II BIOPSY GUIDE?

The FDA 510(k) record lists Rapid Machine & Tool Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAP II BIOPSY GUIDE?

The FDA product code for DAP II BIOPSY GUIDE is HAW.

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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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