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FDA 510(k)

RIGID SUCTION TIPS & RELATED ITEMS

K-Number: K822010 · 1982-08-12

Decision Date1982-08-12
Product CodeJZF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RIGID SUCTION TIPS & RELATED ITEMS is the device name listed in this FDA 510(k) record. The listed applicant is Kelleher Corp.. It received FDA 510(k) clearance on 1982-08-12 under 510(k) number K822010. The device is classified under product code JZF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIGID SUCTION TIPS & RELATED ITEMS?

RIGID SUCTION TIPS & RELATED ITEMS is a medical device that received FDA 510(k) clearance on 1982-08-12. The listed applicant is Kelleher Corp.. The 510(k) number is K822010.

When did RIGID SUCTION TIPS & RELATED ITEMS receive FDA 510(k) clearance?

RIGID SUCTION TIPS & RELATED ITEMS received FDA 510(k) clearance on 1982-08-12, under 510(k) number K822010.

Who is the listed applicant for RIGID SUCTION TIPS & RELATED ITEMS?

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 RIGID SUCTION TIPS & RELATED ITEMS?

The FDA product code for RIGID SUCTION TIPS & RELATED ITEMS is JZF.

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: JZF)

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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