FDA 510(k)

BAL CATH

K-Number: K923487 · 1993-07-30

Decision Date1993-07-30

Product CodeKTR

Advisory CommitteeEN

DecisionUnknown

Device Summary

BAL CATH is the device name listed in this FDA 510(k) record. The listed applicant is Ballard Medical Products. It received FDA 510(k) clearance on 1993-07-30 under 510(k) number K923487. The device is classified under product code KTR. It was reviewed by the EN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BAL CATH?

BAL CATH is a medical device that received FDA 510(k) clearance on 1993-07-30. The listed applicant is Ballard Medical Products. The 510(k) number is K923487.

When did BAL CATH receive FDA 510(k) clearance?

BAL CATH received FDA 510(k) clearance on 1993-07-30, under 510(k) number K923487.

Who is the listed applicant for BAL CATH?

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

What is the FDA product code for BAL CATH?

The FDA product code for BAL CATH is KTR.

Other records listing Ballard Medical Products 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.

K030721QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE K022398REUSABLE BRONCHIAL BIOPSY FORCEPS K013892LUTZ NEEDLE K000495BALLARD MEDICAL PRODUCTS EPIDURAL AND SPINAL NEEDLES K993138BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT K990376BALLARD MEDICAL PRODUCTS FACILETOME BOW STRING PAPILLOTOME

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Related Devices (Code: KTR)

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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.