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FDA 510(k)

LD-1

K-Number: K900107 · 1990-01-18

ApplicantBoehringer Mannheim Corp.
Decision Date1990-01-18
Product CodeDET
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LD-1 is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1990-01-18 under 510(k) number K900107. The device is classified under product code DET. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LD-1?

LD-1 is a medical device that received FDA 510(k) clearance on 1990-01-18. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K900107.

When did LD-1 receive FDA 510(k) clearance?

LD-1 received FDA 510(k) clearance on 1990-01-18, under 510(k) number K900107.

Who is the listed applicant for LD-1?

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

What is the FDA product code for LD-1?

The FDA product code for LD-1 is DET.

Other records listing Boehringer Mannheim 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.

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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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