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FDA 510(k)

VACU-PREP

K-Number: K864923 · 1987-01-20

ApplicantDiversified High Tech Co.
Decision Date1987-01-20
Product Code
DecisionSubstantially Equivalent

Device Summary

VACU-PREP is the device name listed in this FDA 510(k) record. The listed applicant is Diversified High Tech Co.. It received FDA 510(k) clearance on 1987-01-20 under 510(k) number K864923. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACU-PREP?

VACU-PREP is a medical device that received FDA 510(k) clearance on 1987-01-20. The listed applicant is Diversified High Tech Co.. The 510(k) number is K864923.

When did VACU-PREP receive FDA 510(k) clearance?

VACU-PREP received FDA 510(k) clearance on 1987-01-20, under 510(k) number K864923.

Who is the listed applicant for VACU-PREP?

The FDA 510(k) record lists Diversified High Tech Co. as the applicant. This does not by itself establish the device manufacturer.

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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