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FDA 510(k)

SP 120 SOPHISTICATE

K-Number: K802251 · 1980-10-23

ApplicantVickers America Medical Corp.
Decision Date1980-10-23
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SP 120 SOPHISTICATE is the device name listed in this FDA 510(k) record. The listed applicant is Vickers America Medical Corp.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802251. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SP 120 SOPHISTICATE?

SP 120 SOPHISTICATE is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K802251.

When did SP 120 SOPHISTICATE receive FDA 510(k) clearance?

SP 120 SOPHISTICATE received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802251.

Who is the listed applicant for SP 120 SOPHISTICATE?

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

What is the FDA product code for SP 120 SOPHISTICATE?

The FDA product code for SP 120 SOPHISTICATE is JQP.

Related Clinical Trials

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Other records listing Vickers America Medical 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.

K840823TREONIC C30K831838LABORATORY DATA MGMT SYSTEM SDMSK830748RESUSCITAIREK830936TREONIC IP5K813239OXYGENAIRE NURING INCUBATORK813238NEOCARE BABY-CONTROLLED INCUBATOR

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Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, Inc.

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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