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FDA 510(k)

MCARTHUR MICROSCOPE PLASTIC VERSION WITH ACC.

K-Number: K854735 · 1985-12-10

Decision Date1985-12-10
Product CodeIBJ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

MCARTHUR MICROSCOPE PLASTIC VERSION WITH ACC. 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 1985-12-10 under 510(k) number K854735. 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 PLASTIC VERSION WITH ACC.?

MCARTHUR MICROSCOPE PLASTIC VERSION WITH ACC. is a medical device that received FDA 510(k) clearance on 1985-12-10. The listed applicant is Portable Medical Laboratories, Inc.. The 510(k) number is K854735.

When did MCARTHUR MICROSCOPE PLASTIC VERSION WITH ACC. receive FDA 510(k) clearance?

MCARTHUR MICROSCOPE PLASTIC VERSION WITH ACC. received FDA 510(k) clearance on 1985-12-10, under 510(k) number K854735.

Who is the listed applicant for MCARTHUR MICROSCOPE PLASTIC VERSION WITH ACC.?

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 PLASTIC VERSION WITH ACC.?

The FDA product code for MCARTHUR MICROSCOPE PLASTIC VERSION WITH ACC. 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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