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FDA 510(k)

FLORIDA PROBE

K-Number: K875076 · 1988-03-10

ApplicantFlorida Probe Corp.
Decision Date1988-03-10
Product CodeEIX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLORIDA PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Florida Probe Corp.. It received FDA 510(k) clearance on 1988-03-10 under 510(k) number K875076. The device is classified under product code EIX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLORIDA PROBE?

FLORIDA PROBE is a medical device that received FDA 510(k) clearance on 1988-03-10. The listed applicant is Florida Probe Corp.. The 510(k) number is K875076.

When did FLORIDA PROBE receive FDA 510(k) clearance?

FLORIDA PROBE received FDA 510(k) clearance on 1988-03-10, under 510(k) number K875076.

Who is the listed applicant for FLORIDA PROBE?

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

What is the FDA product code for FLORIDA PROBE?

The FDA product code for FLORIDA PROBE is EIX.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Florida Probe 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.

K890493FLORIDA PROBE PERIODONTAL PROBE

Related Devices (Code: EIX)

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.

K960245VIP VICTOR INTERACTIVE PROBEPro-DentecK944848THE VIVACARE T.P.S. PROBERms Div.K936221PROBE TIP/PERI PROBE/PERI PROBE COMP.Pd International ABK890333ALBUMIN REAGENTAlpkem Corp.K880827ACCUTEK PERIODONTAL PROBESweet Micro Systems, Inc.K870280ACCUDENT ACCUPROBEAccudent, Inc.

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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