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FDA 510(k)

CHARLES MICRO PROBE

K-Number: K812857 · 1982-02-05

ApplicantMid Laboratories, Inc.
Decision Date1982-02-05
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CHARLES MICRO PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Mid Laboratories, Inc.. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K812857. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHARLES MICRO PROBE?

CHARLES MICRO PROBE is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Mid Laboratories, Inc.. The 510(k) number is K812857.

When did CHARLES MICRO PROBE receive FDA 510(k) clearance?

CHARLES MICRO PROBE received FDA 510(k) clearance on 1982-02-05, under 510(k) number K812857.

Who is the listed applicant for CHARLES MICRO PROBE?

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

What is the FDA product code for CHARLES MICRO PROBE?

The FDA product code for CHARLES MICRO PROBE is HQE.

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Other records listing Mid Laboratories, Inc. as applicant

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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Related Devices (Code: HQE)

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

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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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