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FDA 510(k)

BALANCED(TM) NYLON BLADDER

K-Number: K930604 · 1993-04-30

ApplicantPymah Corp.
Decision Date1993-04-30
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BALANCED(TM) NYLON BLADDER is the device name listed in this FDA 510(k) record. The listed applicant is Pymah Corp.. It received FDA 510(k) clearance on 1993-04-30 under 510(k) number K930604. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BALANCED(TM) NYLON BLADDER?

BALANCED(TM) NYLON BLADDER is a medical device that received FDA 510(k) clearance on 1993-04-30. The listed applicant is Pymah Corp.. The 510(k) number is K930604.

When did BALANCED(TM) NYLON BLADDER receive FDA 510(k) clearance?

BALANCED(TM) NYLON BLADDER received FDA 510(k) clearance on 1993-04-30, under 510(k) number K930604.

Who is the listed applicant for BALANCED(TM) NYLON BLADDER?

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

What is the FDA product code for BALANCED(TM) NYLON BLADDER?

The FDA product code for BALANCED(TM) NYLON BLADDER is DXQ.

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Related Devices (Code: DXQ)

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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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