DEKA JR.
K-Number: K863204 · 1986-09-03
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Device Summary
Frequently Asked Questions
What is the DEKA JR.?
DEKA JR. is a medical device that received FDA 510(k) clearance on 1986-09-03. The listed applicant is Deka Research & Development Corp.. The 510(k) number is K863204.
When did DEKA JR. receive FDA 510(k) clearance?
DEKA JR. received FDA 510(k) clearance on 1986-09-03, under 510(k) number K863204.
Who is the listed applicant for DEKA JR.?
The FDA 510(k) record lists Deka Research & Development Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEKA JR.?
The FDA product code for DEKA JR. is LDR.
Other records listing Deka Research & Development 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.
Related Devices (Code: LDR)
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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