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FDA 510(k)

ANABAG

K-Number: K871238 · 1987-04-03

Decision Date1987-04-03
Product CodeKZJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANABAG is the device name listed in this FDA 510(k) record. The listed applicant is Scott Laboratories, Inc.. It received FDA 510(k) clearance on 1987-04-03 under 510(k) number K871238. The device is classified under product code KZJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANABAG?

ANABAG is a medical device that received FDA 510(k) clearance on 1987-04-03. The listed applicant is Scott Laboratories, Inc.. The 510(k) number is K871238.

When did ANABAG receive FDA 510(k) clearance?

ANABAG received FDA 510(k) clearance on 1987-04-03, under 510(k) number K871238.

Who is the listed applicant for ANABAG?

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

What is the FDA product code for ANABAG?

The FDA product code for ANABAG is KZJ.

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 Scott 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 16 devices →

Related Devices (Code: KZJ)

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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