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FDA 510(k)

HOMER MAMMALOK LOCALIZATION SHIELD

K-Number: K885090 · 1989-02-14

Decision Date1989-02-14
Product CodeLRO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOMER MAMMALOK LOCALIZATION SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is North American Instrument Corp.. It received FDA 510(k) clearance on 1989-02-14 under 510(k) number K885090. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOMER MAMMALOK LOCALIZATION SHIELD?

HOMER MAMMALOK LOCALIZATION SHIELD is a medical device that received FDA 510(k) clearance on 1989-02-14. The listed applicant is North American Instrument Corp.. The 510(k) number is K885090.

When did HOMER MAMMALOK LOCALIZATION SHIELD receive FDA 510(k) clearance?

HOMER MAMMALOK LOCALIZATION SHIELD received FDA 510(k) clearance on 1989-02-14, under 510(k) number K885090.

Who is the listed applicant for HOMER MAMMALOK LOCALIZATION SHIELD?

The FDA 510(k) record lists North American Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOMER MAMMALOK LOCALIZATION SHIELD?

The FDA product code for HOMER MAMMALOK LOCALIZATION SHIELD is LRO.

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 North American Instrument Corp. 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 28 devices →

Related Devices (Code: LRO)

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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