LAPOROTOMY SPONGE
K-Number: K780806 · 1978-06-22
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Device Summary
Frequently Asked Questions
What is the LAPOROTOMY SPONGE?
LAPOROTOMY SPONGE is a medical device that received FDA 510(k) clearance on 1978-06-22. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K780806.
When did LAPOROTOMY SPONGE receive FDA 510(k) clearance?
LAPOROTOMY SPONGE received FDA 510(k) clearance on 1978-06-22, under 510(k) number K780806.
Who is the listed applicant for LAPOROTOMY SPONGE?
The FDA 510(k) record lists Abco Dealers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAPOROTOMY SPONGE?
The FDA product code for LAPOROTOMY SPONGE is EFQ.
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 Abco Dealers, 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: EFQ)
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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