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FDA 510(k)

SPECBOARD

K-Number: K891090 · 1989-04-07

Decision Date1989-04-07
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SPECBOARD is the device name listed in this FDA 510(k) record. The listed applicant is Macbrud Corp. Medical Div.. It received FDA 510(k) clearance on 1989-04-07 under 510(k) number K891090. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECBOARD?

SPECBOARD is a medical device that received FDA 510(k) clearance on 1989-04-07. The listed applicant is Macbrud Corp. Medical Div.. The 510(k) number is K891090.

When did SPECBOARD receive FDA 510(k) clearance?

SPECBOARD received FDA 510(k) clearance on 1989-04-07, under 510(k) number K891090.

Who is the listed applicant for SPECBOARD?

The FDA 510(k) record lists Macbrud Corp. Medical Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECBOARD?

The FDA product code for SPECBOARD is IZH.

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 Macbrud Corp. Medical Div. 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.

Related Devices (Code: IZH)

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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