FDA 510(k)

OCCUPAK CAT.#200-0538

K-Number: K802691 · 1980-10-27

Decision Date1980-10-27

Product Code

DecisionUnknown

Device Summary

OCCUPAK CAT.#200-0538 is the device name listed in this FDA 510(k) record. The listed applicant is Occumedics, Inc.. It received FDA 510(k) clearance on 1980-10-27 under 510(k) number K802691. FDA Decision: Unknown.

Frequently Asked Questions

What is the OCCUPAK CAT.#200-0538?

OCCUPAK CAT.#200-0538 is a medical device that received FDA 510(k) clearance on 1980-10-27. The listed applicant is Occumedics, Inc.. The 510(k) number is K802691.

When did OCCUPAK CAT.#200-0538 receive FDA 510(k) clearance?

OCCUPAK CAT.#200-0538 received FDA 510(k) clearance on 1980-10-27, under 510(k) number K802691.

Who is the listed applicant for OCCUPAK CAT.#200-0538?

The FDA 510(k) record lists Occumedics, Inc. 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 Occumedics, Inc. as applicant

K802690ULTRAPAK CAT. #100-0251

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.