FDA 510(k)

VACU-GUARD

K-Number: K863162 · 1986-08-29

Decision Date1986-08-29

Product Code

DecisionSubstantially Equivalent

Device Summary

VACU-GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Arbor Technologies, Inc.. It received FDA 510(k) clearance on 1986-08-29 under 510(k) number K863162. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACU-GUARD?

VACU-GUARD is a medical device that received FDA 510(k) clearance on 1986-08-29. The listed applicant is Arbor Technologies, Inc.. The 510(k) number is K863162.

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

VACU-GUARD received FDA 510(k) clearance on 1986-08-29, under 510(k) number K863162.

Who is the listed applicant for VACU-GUARD?

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

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Other records listing Arbor Technologies, Inc. as applicant

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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.