CLINIFLOW II, #701, ELECTROMAGN. BLD. SY
K-Number: K820272 · 1982-03-12
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Device Summary
Frequently Asked Questions
What is the CLINIFLOW II, #701, ELECTROMAGN. BLD. SY?
CLINIFLOW II, #701, ELECTROMAGN. BLD. SY is a medical device that received FDA 510(k) clearance on 1982-03-12. The listed applicant is Carolina Medical Electronics. The 510(k) number is K820272.
When did CLINIFLOW II, #701, ELECTROMAGN. BLD. SY receive FDA 510(k) clearance?
CLINIFLOW II, #701, ELECTROMAGN. BLD. SY received FDA 510(k) clearance on 1982-03-12, under 510(k) number K820272.
Who is the listed applicant for CLINIFLOW II, #701, ELECTROMAGN. BLD. SY?
The FDA 510(k) record lists Carolina Medical Electronics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLINIFLOW II, #701, ELECTROMAGN. BLD. SY?
The FDA product code for CLINIFLOW II, #701, ELECTROMAGN. BLD. SY is DPW.
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 Carolina Medical Electronics 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: DPW)
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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