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FDA 510(k)

BAUMAN RIGID LARYNGOSCOPE

K-Number: K901680 · 1990-07-12

ApplicantPalex Intl. SA
Decision Date1990-07-12
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BAUMAN RIGID LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Palex Intl. SA. It received FDA 510(k) clearance on 1990-07-12 under 510(k) number K901680. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAUMAN RIGID LARYNGOSCOPE?

BAUMAN RIGID LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1990-07-12. The listed applicant is Palex Intl. SA. The 510(k) number is K901680.

When did BAUMAN RIGID LARYNGOSCOPE receive FDA 510(k) clearance?

BAUMAN RIGID LARYNGOSCOPE received FDA 510(k) clearance on 1990-07-12, under 510(k) number K901680.

Who is the listed applicant for BAUMAN RIGID LARYNGOSCOPE?

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

What is the FDA product code for BAUMAN RIGID LARYNGOSCOPE?

The FDA product code for BAUMAN RIGID LARYNGOSCOPE is CCW.

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 Palex Intl. SA 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.

K905108CONTORNO(R), MODELS E AND STK904586PALEX IRRIGATION SETK903224EPISENSORK902642CONTORNO (TM)

Related Devices (Code: CCW)

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.

K191602APA Oxy BladeVenner Medical (Singapore) Pte, Ltd.K163412Girgis Scope Video 200 Double Bladed Laryngoscope (GSV200.DBL)Girgis Scope, LLCK121378AIRTRAQ SP AIRTRAQ AVANTProdol Meditec , Ltd.K063477NOVAMED MRI CONDITIONAL LARYNGOSCOPE SETNovamed, LLCK062523TRU-MR LARYNGOSCOPE SETTruphatek International, Ltd.K062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002Minrad, Inc.

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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