NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS
K-Number: K851508 · 1985-07-12
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Device Summary
Frequently Asked Questions
What is the NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS?
NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS is a medical device that received FDA 510(k) clearance on 1985-07-12. The listed applicant is Nikon, Inc.. The 510(k) number is K851508.
When did NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS receive FDA 510(k) clearance?
NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS received FDA 510(k) clearance on 1985-07-12, under 510(k) number K851508.
Who is the listed applicant for NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS?
The FDA 510(k) record lists Nikon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS?
The FDA product code for NIKON/JOYCE LOCK MAGICAN 2 CHROMOSOME SYS is LNJ.
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 Nikon, 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.
Related Devices (Code: LNJ)
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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