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FDA 510(k)

BAG-TAIL BLEED VALVE

K-Number: K870859 · 1987-08-03

ApplicantDryden Corp.
Decision Date1987-08-03
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BAG-TAIL BLEED VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1987-08-03 under 510(k) number K870859. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAG-TAIL BLEED VALVE?

BAG-TAIL BLEED VALVE is a medical device that received FDA 510(k) clearance on 1987-08-03. The listed applicant is Dryden Corp.. The 510(k) number is K870859.

When did BAG-TAIL BLEED VALVE receive FDA 510(k) clearance?

BAG-TAIL BLEED VALVE received FDA 510(k) clearance on 1987-08-03, under 510(k) number K870859.

Who is the listed applicant for BAG-TAIL BLEED VALVE?

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 BAG-TAIL BLEED VALVE?

The FDA product code for BAG-TAIL BLEED VALVE is CAI.

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Other records listing Dryden Corp. as applicant

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Related Devices (Code: CAI)

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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