DISP. ABSORBENT COMPRESSED FIBRE WAFER
K-Number: K770063 · 1977-01-14
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Device Summary
Frequently Asked Questions
What is the DISP. ABSORBENT COMPRESSED FIBRE WAFER?
DISP. ABSORBENT COMPRESSED FIBRE WAFER is a medical device that received FDA 510(k) clearance on 1977-01-14. The listed applicant is Lorvic Corp.. The 510(k) number is K770063.
When did DISP. ABSORBENT COMPRESSED FIBRE WAFER receive FDA 510(k) clearance?
DISP. ABSORBENT COMPRESSED FIBRE WAFER received FDA 510(k) clearance on 1977-01-14, under 510(k) number K770063.
Who is the listed applicant for DISP. ABSORBENT COMPRESSED FIBRE WAFER?
The FDA 510(k) record lists Lorvic Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISP. ABSORBENT COMPRESSED FIBRE WAFER?
The FDA product code for DISP. ABSORBENT COMPRESSED FIBRE WAFER is EFN.
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 Lorvic 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: EFN)
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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