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FDA 510(k)

CATHETER IRRIGATION SYRINGES, #3100,3110

K-Number: K801781 · 1980-08-13

Decision Date1980-08-13
Product CodeKQT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER IRRIGATION SYRINGES, #3100,3110 is the device name listed in this FDA 510(k) record. The listed applicant is The Healthcare Group Laboratories, Inc.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801781. The device is classified under product code KQT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER IRRIGATION SYRINGES, #3100,3110?

CATHETER IRRIGATION SYRINGES, #3100,3110 is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K801781.

When did CATHETER IRRIGATION SYRINGES, #3100,3110 receive FDA 510(k) clearance?

CATHETER IRRIGATION SYRINGES, #3100,3110 received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801781.

Who is the listed applicant for CATHETER IRRIGATION SYRINGES, #3100,3110?

The FDA 510(k) record lists The Healthcare Group Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER IRRIGATION SYRINGES, #3100,3110?

The FDA product code for CATHETER IRRIGATION SYRINGES, #3100,3110 is KQT.

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 The Healthcare Group Laboratories, Inc. 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 29 devices →

Related Devices (Code: KQT)

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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