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FDA 510(k)

CAMERON-MILLER #40-1516

K-Number: K822092 · 1982-09-21

ApplicantCameron-Miller, Inc.
Decision Date1982-09-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAMERON-MILLER #40-1516 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 1982-09-21 under 510(k) number K822092. 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 CAMERON-MILLER #40-1516?

CAMERON-MILLER #40-1516 is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is Cameron-Miller, Inc.. The 510(k) number is K822092.

When did CAMERON-MILLER #40-1516 receive FDA 510(k) clearance?

CAMERON-MILLER #40-1516 received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822092.

Who is the listed applicant for CAMERON-MILLER #40-1516?

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 CAMERON-MILLER #40-1516?

The FDA product code for CAMERON-MILLER #40-1516 is GEI.

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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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