PANAMEDIC GAUZE SPONGES
K-Number: K850093 · 1985-02-21
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Device Summary
Frequently Asked Questions
What is the PANAMEDIC GAUZE SPONGES?
PANAMEDIC GAUZE SPONGES is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is General Electric Trading Co.. The 510(k) number is K850093.
When did PANAMEDIC GAUZE SPONGES receive FDA 510(k) clearance?
PANAMEDIC GAUZE SPONGES received FDA 510(k) clearance on 1985-02-21, under 510(k) number K850093.
Who is the listed applicant for PANAMEDIC GAUZE SPONGES?
The FDA 510(k) record lists General Electric Trading Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PANAMEDIC GAUZE SPONGES?
The FDA product code for PANAMEDIC GAUZE SPONGES 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 Electric Trading 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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