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FDA 510(k)

DR. FOG

K-Number: K932449 · 1993-08-11

ApplicantO.R. Concepts, Inc.
Decision Date1993-08-11
Product CodeOCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DR. FOG is the device name listed in this FDA 510(k) record. The listed applicant is O.R. Concepts, Inc.. It received FDA 510(k) clearance on 1993-08-11 under 510(k) number K932449. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR. FOG?

DR. FOG is a medical device that received FDA 510(k) clearance on 1993-08-11. The listed applicant is O.R. Concepts, Inc.. The 510(k) number is K932449.

When did DR. FOG receive FDA 510(k) clearance?

DR. FOG received FDA 510(k) clearance on 1993-08-11, under 510(k) number K932449.

Who is the listed applicant for DR. FOG?

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

What is the FDA product code for DR. FOG?

The FDA product code for DR. FOG is OCT.

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Related Devices (Code: OCT)

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.

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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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