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FDA 510(k)

TECHNICATOR

K-Number: K812702 · 1981-11-05

ApplicantCameron-Miller, Inc.
Decision Date1981-11-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TECHNICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cameron-Miller, Inc.. It received FDA 510(k) clearance on 1981-11-05 under 510(k) number K812702. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICATOR?

TECHNICATOR is a medical device that received FDA 510(k) clearance on 1981-11-05. The listed applicant is Cameron-Miller, Inc.. The 510(k) number is K812702.

When did TECHNICATOR receive FDA 510(k) clearance?

TECHNICATOR received FDA 510(k) clearance on 1981-11-05, under 510(k) number K812702.

Who is the listed applicant for TECHNICATOR?

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

What is the FDA product code for TECHNICATOR?

The FDA product code for TECHNICATOR is GEI.

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Other records listing Cameron-Miller, Inc. as applicant

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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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