FDA 510(k)

SOC SLIDE CULTURE SYSTEM

K-Number: K882371 · 1988-07-18

ApplicantThe Cancer Center AT Wadley Institutes

Decision Date1988-07-18

Product CodeJXC

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SOC SLIDE CULTURE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is The Cancer Center AT Wadley Institutes. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K882371. The device is classified under product code JXC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOC SLIDE CULTURE SYSTEM?

SOC SLIDE CULTURE SYSTEM is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is The Cancer Center AT Wadley Institutes. The 510(k) number is K882371.

When did SOC SLIDE CULTURE SYSTEM receive FDA 510(k) clearance?

SOC SLIDE CULTURE SYSTEM received FDA 510(k) clearance on 1988-07-18, under 510(k) number K882371.

Who is the listed applicant for SOC SLIDE CULTURE SYSTEM?

The FDA 510(k) record lists The Cancer Center AT Wadley Institutes as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOC SLIDE CULTURE SYSTEM?

The FDA product code for SOC SLIDE CULTURE SYSTEM is JXC.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: JXC)

K960075CHROMAGAR CANDIDAHardy Diagnostics K913426ALBICANS SUREJrga Diagnostics K884720GERM TUBE SOLUTIONRemel Co.K891476C. ALBICANS SCREENCarr-Scarborough Microbiologicals, Inc.K832406QUANTUM II YEAST IDENT. SYSTEMAbbott Laboratories

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.