PROGRAMMABLE STIMULATOR 2352
K-Number: K833421 · 1984-01-30
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Device Summary
Frequently Asked Questions
What is the PROGRAMMABLE STIMULATOR 2352?
PROGRAMMABLE STIMULATOR 2352 is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Medtronic Vascular. The 510(k) number is K833421.
When did PROGRAMMABLE STIMULATOR 2352 receive FDA 510(k) clearance?
PROGRAMMABLE STIMULATOR 2352 received FDA 510(k) clearance on 1984-01-30, under 510(k) number K833421.
Who is the listed applicant for PROGRAMMABLE STIMULATOR 2352?
The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROGRAMMABLE STIMULATOR 2352?
The FDA product code for PROGRAMMABLE STIMULATOR 2352 is JOQ.
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.
Other records listing Medtronic Vascular 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.
Related Devices (Code: JOQ)
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.
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.
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