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FDA 510(k)

MCARTHUR MICROSCOPE, STANDARD METAL VERSION

K-Number: K864049 · 1986-10-29

Decision Date1986-10-29
Product CodeIBJ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

MCARTHUR MICROSCOPE, STANDARD METAL VERSION is the device name listed in this FDA 510(k) record. The listed applicant is Portable Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1986-10-29 under 510(k) number K864049. The device is classified under product code IBJ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCARTHUR MICROSCOPE, STANDARD METAL VERSION?

MCARTHUR MICROSCOPE, STANDARD METAL VERSION is a medical device that received FDA 510(k) clearance on 1986-10-29. The listed applicant is Portable Medical Laboratories, Inc.. The 510(k) number is K864049.

When did MCARTHUR MICROSCOPE, STANDARD METAL VERSION receive FDA 510(k) clearance?

MCARTHUR MICROSCOPE, STANDARD METAL VERSION received FDA 510(k) clearance on 1986-10-29, under 510(k) number K864049.

Who is the listed applicant for MCARTHUR MICROSCOPE, STANDARD METAL VERSION?

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

What is the FDA product code for MCARTHUR MICROSCOPE, STANDARD METAL VERSION?

The FDA product code for MCARTHUR MICROSCOPE, STANDARD METAL VERSION is IBJ.

Related Clinical Trials

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.

Other records listing Portable Medical 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.

View all 9 devices →

Related Devices (Code: IBJ)

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.

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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