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FDA 510(k)

VISTA INSTRUMENT

K-Number: K882914 · 1988-08-30

ApplicantAbbott Laboratories
Decision Date1988-08-30
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VISTA INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1988-08-30 under 510(k) number K882914. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTA INSTRUMENT?

VISTA INSTRUMENT is a medical device that received FDA 510(k) clearance on 1988-08-30. The listed applicant is Abbott Laboratories. The 510(k) number is K882914.

When did VISTA INSTRUMENT receive FDA 510(k) clearance?

VISTA INSTRUMENT received FDA 510(k) clearance on 1988-08-30, under 510(k) number K882914.

Who is the listed applicant for VISTA INSTRUMENT?

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

What is the FDA product code for VISTA INSTRUMENT?

The FDA product code for VISTA INSTRUMENT is JJE.

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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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