LAPAROTOMY SPOGNE
K-Number: K772089 · 1977-11-11
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Device Summary
Frequently Asked Questions
What is the LAPAROTOMY SPOGNE?
LAPAROTOMY SPOGNE is a medical device that received FDA 510(k) clearance on 1977-11-11. The listed applicant is General Medical Co.. The 510(k) number is K772089.
When did LAPAROTOMY SPOGNE receive FDA 510(k) clearance?
LAPAROTOMY SPOGNE received FDA 510(k) clearance on 1977-11-11, under 510(k) number K772089.
Who is the listed applicant for LAPAROTOMY SPOGNE?
The FDA 510(k) record lists General Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAPAROTOMY SPOGNE?
The FDA product code for LAPAROTOMY SPOGNE 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 General Medical Co. 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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