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FDA 510(k)

ENDOSCOPIC SPONGE CARRIER

K-Number: K822194 · 1982-08-27

Decision Date1982-08-27
Product CodeFGS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC SPONGE CARRIER is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-27 under 510(k) number K822194. The device is classified under product code FGS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC SPONGE CARRIER?

ENDOSCOPIC SPONGE CARRIER is a medical device that received FDA 510(k) clearance on 1982-08-27. The listed applicant is Kelleher Corp.. The 510(k) number is K822194.

When did ENDOSCOPIC SPONGE CARRIER receive FDA 510(k) clearance?

ENDOSCOPIC SPONGE CARRIER received FDA 510(k) clearance on 1982-08-27, under 510(k) number K822194.

Who is the listed applicant for ENDOSCOPIC SPONGE CARRIER?

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 ENDOSCOPIC SPONGE CARRIER?

The FDA product code for ENDOSCOPIC SPONGE CARRIER is FGS.

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.

View all 94 devices →

Related Devices (Code: FGS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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