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FDA 510(k)

5.0 IOP & 7.5 IOP PROBES

K-Number: K853432 · 1986-02-07

ApplicantDiasonics, Inc.
Decision Date1986-02-07
Product CodeGXW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

5.0 IOP & 7.5 IOP PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Diasonics, Inc.. It received FDA 510(k) clearance on 1986-02-07 under 510(k) number K853432. The device is classified under product code GXW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5.0 IOP & 7.5 IOP PROBES?

5.0 IOP & 7.5 IOP PROBES is a medical device that received FDA 510(k) clearance on 1986-02-07. The listed applicant is Diasonics, Inc.. The 510(k) number is K853432.

When did 5.0 IOP & 7.5 IOP PROBES receive FDA 510(k) clearance?

5.0 IOP & 7.5 IOP PROBES received FDA 510(k) clearance on 1986-02-07, under 510(k) number K853432.

Who is the listed applicant for 5.0 IOP & 7.5 IOP PROBES?

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

What is the FDA product code for 5.0 IOP & 7.5 IOP PROBES?

The FDA product code for 5.0 IOP & 7.5 IOP PROBES is GXW.

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Related Devices (Code: GXW)

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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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