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FDA 510(k)

BADGWELL SAMPLING CATHETER

K-Number: K870858 · 1987-05-14

ApplicantDryden Corp.
Decision Date1987-05-14
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BADGWELL SAMPLING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1987-05-14 under 510(k) number K870858. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BADGWELL SAMPLING CATHETER?

BADGWELL SAMPLING CATHETER is a medical device that received FDA 510(k) clearance on 1987-05-14. The listed applicant is Dryden Corp.. The 510(k) number is K870858.

When did BADGWELL SAMPLING CATHETER receive FDA 510(k) clearance?

BADGWELL SAMPLING CATHETER received FDA 510(k) clearance on 1987-05-14, under 510(k) number K870858.

Who is the listed applicant for BADGWELL SAMPLING CATHETER?

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

What is the FDA product code for BADGWELL SAMPLING CATHETER?

The FDA product code for BADGWELL SAMPLING CATHETER is CCK.

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 Dryden 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 21 devices →

Related Devices (Code: CCK)

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

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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