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FDA 510(k)

INPERSOL CAPD ADMIN. SET & CATHETER ADAP

K-Number: K800993 · 1980-08-12

ApplicantAbbott Laboratories
Decision Date1980-08-12
Product CodeKDJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INPERSOL CAPD ADMIN. SET & CATHETER ADAP is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1980-08-12 under 510(k) number K800993. The device is classified under product code KDJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INPERSOL CAPD ADMIN. SET & CATHETER ADAP?

INPERSOL CAPD ADMIN. SET & CATHETER ADAP is a medical device that received FDA 510(k) clearance on 1980-08-12. The listed applicant is Abbott Laboratories. The 510(k) number is K800993.

When did INPERSOL CAPD ADMIN. SET & CATHETER ADAP receive FDA 510(k) clearance?

INPERSOL CAPD ADMIN. SET & CATHETER ADAP received FDA 510(k) clearance on 1980-08-12, under 510(k) number K800993.

Who is the listed applicant for INPERSOL CAPD ADMIN. SET & CATHETER ADAP?

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

What is the FDA product code for INPERSOL CAPD ADMIN. SET & CATHETER ADAP?

The FDA product code for INPERSOL CAPD ADMIN. SET & CATHETER ADAP is KDJ.

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Related Devices (Code: KDJ)

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.

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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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