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FDA 510(k)

PANCRETEC PUMP CHECK

K-Number: K841018 · 1984-04-05

ApplicantPancretec, Inc.
Decision Date1984-04-05
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PANCRETEC PUMP CHECK is the device name listed in this FDA 510(k) record. The listed applicant is Pancretec, Inc.. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K841018. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANCRETEC PUMP CHECK?

PANCRETEC PUMP CHECK is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Pancretec, Inc.. The 510(k) number is K841018.

When did PANCRETEC PUMP CHECK receive FDA 510(k) clearance?

PANCRETEC PUMP CHECK received FDA 510(k) clearance on 1984-04-05, under 510(k) number K841018.

Who is the listed applicant for PANCRETEC PUMP CHECK?

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

What is the FDA product code for PANCRETEC PUMP CHECK?

The FDA product code for PANCRETEC PUMP CHECK is FRN.

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Other records listing Pancretec, 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.

K882102PROVIDER ONE INFUSION SYSTEMK871806PROVIDER IV. MODEL 5000 INFUSION DEVICEK844078PROVIDER PA 3000 INFUSION SYSTEMK843463PROVIDER BAG SPIKE W/12 MICROBORE EXTENK841373PROVIDER IV MODEL 2000 INFUSIN SYSK841017PROVIDER INFUSION SET

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Related Devices (Code: FRN)

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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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