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FDA 510(k)

PROBE TIP/PERI PROBE/PERI PROBE COMP.

K-Number: K936221 · 1994-08-01

ApplicantPd International AB
Decision Date1994-08-01
Product CodeEIX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROBE TIP/PERI PROBE/PERI PROBE COMP. is the device name listed in this FDA 510(k) record. The listed applicant is Pd International AB. It received FDA 510(k) clearance on 1994-08-01 under 510(k) number K936221. 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 PROBE TIP/PERI PROBE/PERI PROBE COMP.?

PROBE TIP/PERI PROBE/PERI PROBE COMP. is a medical device that received FDA 510(k) clearance on 1994-08-01. The listed applicant is Pd International AB. The 510(k) number is K936221.

When did PROBE TIP/PERI PROBE/PERI PROBE COMP. receive FDA 510(k) clearance?

PROBE TIP/PERI PROBE/PERI PROBE COMP. received FDA 510(k) clearance on 1994-08-01, under 510(k) number K936221.

Who is the listed applicant for PROBE TIP/PERI PROBE/PERI PROBE COMP.?

The FDA 510(k) record lists Pd International AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROBE TIP/PERI PROBE/PERI PROBE COMP.?

The FDA product code for PROBE TIP/PERI PROBE/PERI PROBE COMP. 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

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.K890333ALBUMIN REAGENTAlpkem Corp.K880827ACCUTEK PERIODONTAL PROBESweet Micro Systems, Inc.K875076FLORIDA PROBEFlorida Probe Corp.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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