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FDA 510(k)

BIO INTERFERENCE BLANKING MATERIAL

K-Number: K823687 · 1983-01-07

Decision Date1983-01-07
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BIO INTERFERENCE BLANKING MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is American Monitor Corp.. It received FDA 510(k) clearance on 1983-01-07 under 510(k) number K823687. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO INTERFERENCE BLANKING MATERIAL?

BIO INTERFERENCE BLANKING MATERIAL is a medical device that received FDA 510(k) clearance on 1983-01-07. The listed applicant is American Monitor Corp.. The 510(k) number is K823687.

When did BIO INTERFERENCE BLANKING MATERIAL receive FDA 510(k) clearance?

BIO INTERFERENCE BLANKING MATERIAL received FDA 510(k) clearance on 1983-01-07, under 510(k) number K823687.

Who is the listed applicant for BIO INTERFERENCE BLANKING MATERIAL?

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

What is the FDA product code for BIO INTERFERENCE BLANKING MATERIAL?

The FDA product code for BIO INTERFERENCE BLANKING MATERIAL is JJX.

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 American Monitor 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 73 devices →

Related Devices (Code: JJX)

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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