EPCOM VCU-1 VACUUM SYSTEM & CURETTE
K-Number: K831112 · 1983-06-30
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Device Summary
Frequently Asked Questions
What is the EPCOM VCU-1 VACUUM SYSTEM & CURETTE?
EPCOM VCU-1 VACUUM SYSTEM & CURETTE is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Epcom Medical Systems, Inc.. The 510(k) number is K831112.
When did EPCOM VCU-1 VACUUM SYSTEM & CURETTE receive FDA 510(k) clearance?
EPCOM VCU-1 VACUUM SYSTEM & CURETTE received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831112.
Who is the listed applicant for EPCOM VCU-1 VACUUM SYSTEM & CURETTE?
The FDA 510(k) record lists Epcom Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EPCOM VCU-1 VACUUM SYSTEM & CURETTE?
The FDA product code for EPCOM VCU-1 VACUUM SYSTEM & CURETTE is HHI.
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 Epcom Medical Systems, 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.
Related Devices (Code: HHI)
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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