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FDA 510(k)

F4912 NIGHT VISION AID

K-Number: K761215 · 1976-12-16

ApplicantItt Corp.
Decision Date1976-12-16
Product CodeHPG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

F4912 NIGHT VISION AID is the device name listed in this FDA 510(k) record. The listed applicant is Itt Corp.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761215. The device is classified under product code HPG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the F4912 NIGHT VISION AID?

F4912 NIGHT VISION AID is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Itt Corp.. The 510(k) number is K761215.

When did F4912 NIGHT VISION AID receive FDA 510(k) clearance?

F4912 NIGHT VISION AID received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761215.

Who is the listed applicant for F4912 NIGHT VISION AID?

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

What is the FDA product code for F4912 NIGHT VISION AID?

The FDA product code for F4912 NIGHT VISION AID is HPG.

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Related Devices (Code: HPG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K910601PATHFINDERNurion IndustriesK910124LOW VISION ENHANCEMENT SYSTEM (LVES)Triangle InvestmentsK903558LASER CANENurion IndustriesK902187POLARONNurion IndustriesK862338SENSORY 6Brytech, Inc.K823385ALESOms

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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