PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST
K-Number: K861974 · 1986-08-04
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Device Summary
Frequently Asked Questions
What is the PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST?
PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST is a medical device that received FDA 510(k) clearance on 1986-08-04. The listed applicant is Perceptive Systems, Inc.. The 510(k) number is K861974.
When did PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST receive FDA 510(k) clearance?
PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST received FDA 510(k) clearance on 1986-08-04, under 510(k) number K861974.
Who is the listed applicant for PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST?
The FDA 510(k) record lists Perceptive Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST?
The FDA product code for PERCEPTIVE SYSTEMS INC PSICOM 217 KARYOTYPING SYST 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 Perceptive Systems, 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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