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FDA 510(k)

LN 100 BREAST MARKER

K-Number: K872319 · 1987-08-11

Decision Date1987-08-11
Product CodeFTY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LN 100 BREAST MARKER is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Industries, Inc.. It received FDA 510(k) clearance on 1987-08-11 under 510(k) number K872319. The device is classified under product code FTY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LN 100 BREAST MARKER?

LN 100 BREAST MARKER is a medical device that received FDA 510(k) clearance on 1987-08-11. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K872319.

When did LN 100 BREAST MARKER receive FDA 510(k) clearance?

LN 100 BREAST MARKER received FDA 510(k) clearance on 1987-08-11, under 510(k) number K872319.

Who is the listed applicant for LN 100 BREAST MARKER?

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

What is the FDA product code for LN 100 BREAST MARKER?

The FDA product code for LN 100 BREAST MARKER is FTY.

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 Instrumentation Industries, 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 45 devices →

Related Devices (Code: FTY)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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