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FDA 510(k)

BODILY FLUID DISPOSAL KIT

K-Number: K961217 · 1996-07-25

ApplicantTransidyne General Corp.
Decision Date1996-07-25
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BODILY FLUID DISPOSAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Transidyne General Corp.. It received FDA 510(k) clearance on 1996-07-25 under 510(k) number K961217. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODILY FLUID DISPOSAL KIT?

BODILY FLUID DISPOSAL KIT is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Transidyne General Corp.. The 510(k) number is K961217.

When did BODILY FLUID DISPOSAL KIT receive FDA 510(k) clearance?

BODILY FLUID DISPOSAL KIT received FDA 510(k) clearance on 1996-07-25, under 510(k) number K961217.

Who is the listed applicant for BODILY FLUID DISPOSAL KIT?

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

What is the FDA product code for BODILY FLUID DISPOSAL KIT?

The FDA product code for BODILY FLUID DISPOSAL KIT is FXX.

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.

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Other records listing Transidyne General 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.

K955658LACERATION TRAYK950743ORAL PROCEDURE PACKK950773PROPHYLAXIS PACKK950449SURGICAL BURK950403SURGICAL SAW BLADESK924811I.V. START KIT

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Related Devices (Code: FXX)

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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