FDA 510(k)

OBSTETRICAL KIT

K-Number: K863504 · 1986-10-22

Decision Date1986-10-22

Product Code

DecisionUnknown

Device Summary

OBSTETRICAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Dyna-Med. It received FDA 510(k) clearance on 1986-10-22 under 510(k) number K863504. FDA Decision: Unknown.

Frequently Asked Questions

What is the OBSTETRICAL KIT?

OBSTETRICAL KIT is a medical device that received FDA 510(k) clearance on 1986-10-22. The listed applicant is Dyna-Med. The 510(k) number is K863504.

When did OBSTETRICAL KIT receive FDA 510(k) clearance?

OBSTETRICAL KIT received FDA 510(k) clearance on 1986-10-22, under 510(k) number K863504.

Who is the listed applicant for OBSTETRICAL KIT?

The FDA 510(k) record lists Dyna-Med as the applicant. This does not by itself establish the device manufacturer.

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

Other records listing Dyna-Med as applicant

K884578POLARIX 2 AND POLARIX 2E K884340AMX-110, AMX-II AND AMX-III K760258BITE STICK, DYNA

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.