SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC.
K-Number: K852180 · 1985-07-01
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Device Summary
Frequently Asked Questions
What is the SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC.?
SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC. is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Surgidyne, Inc.. The 510(k) number is K852180.
When did SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC. receive FDA 510(k) clearance?
SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC. received FDA 510(k) clearance on 1985-07-01, under 510(k) number K852180.
Who is the listed applicant for SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC.?
The FDA 510(k) record lists Surgidyne, 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.
Other records listing Surgidyne, Inc. 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.
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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