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FDA 510(k)

VIGGO EXACTA PRESSURE MONITORING KIT

K-Number: K864900 · 1987-04-01

ApplicantOhmeda Medical
Decision Date1987-04-01
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VIGGO EXACTA PRESSURE MONITORING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1987-04-01 under 510(k) number K864900. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIGGO EXACTA PRESSURE MONITORING KIT?

VIGGO EXACTA PRESSURE MONITORING KIT is a medical device that received FDA 510(k) clearance on 1987-04-01. The listed applicant is Ohmeda Medical. The 510(k) number is K864900.

When did VIGGO EXACTA PRESSURE MONITORING KIT receive FDA 510(k) clearance?

VIGGO EXACTA PRESSURE MONITORING KIT received FDA 510(k) clearance on 1987-04-01, under 510(k) number K864900.

Who is the listed applicant for VIGGO EXACTA PRESSURE MONITORING KIT?

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

What is the FDA product code for VIGGO EXACTA PRESSURE MONITORING KIT?

The FDA product code for VIGGO EXACTA PRESSURE MONITORING KIT is FMG.

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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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