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FDA 510(k)

SALTER VOLUCHEK 6600

K-Number: K863656 · 1986-10-06

ApplicantSalter Labs
Decision Date1986-10-06
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SALTER VOLUCHEK 6600 is the device name listed in this FDA 510(k) record. The listed applicant is Salter Labs. It received FDA 510(k) clearance on 1986-10-06 under 510(k) number K863656. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALTER VOLUCHEK 6600?

SALTER VOLUCHEK 6600 is a medical device that received FDA 510(k) clearance on 1986-10-06. The listed applicant is Salter Labs. The 510(k) number is K863656.

When did SALTER VOLUCHEK 6600 receive FDA 510(k) clearance?

SALTER VOLUCHEK 6600 received FDA 510(k) clearance on 1986-10-06, under 510(k) number K863656.

Who is the listed applicant for SALTER VOLUCHEK 6600?

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

What is the FDA product code for SALTER VOLUCHEK 6600?

The FDA product code for SALTER VOLUCHEK 6600 is BZG.

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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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