FORCEPS FOR USE WITH RIGID ENDOSCOPES
K-Number: K822193 · 1982-08-24
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Device Summary
Frequently Asked Questions
What is the FORCEPS FOR USE WITH RIGID ENDOSCOPES?
FORCEPS FOR USE WITH RIGID ENDOSCOPES is a medical device that received FDA 510(k) clearance on 1982-08-24. The listed applicant is Kelleher Corp.. The 510(k) number is K822193.
When did FORCEPS FOR USE WITH RIGID ENDOSCOPES receive FDA 510(k) clearance?
FORCEPS FOR USE WITH RIGID ENDOSCOPES received FDA 510(k) clearance on 1982-08-24, under 510(k) number K822193.
Who is the listed applicant for FORCEPS FOR USE WITH RIGID ENDOSCOPES?
The FDA 510(k) record lists Kelleher Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORCEPS FOR USE WITH RIGID ENDOSCOPES?
The FDA product code for FORCEPS FOR USE WITH RIGID ENDOSCOPES is JEK.
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 Kelleher 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: JEK)
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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