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FDA 510(k)

CLM LARYNGOSCOPE

K-Number: K953179 · 1995-10-06

ApplicantPenlon , Ltd.
Decision Date1995-10-06
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CLM LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Penlon , Ltd.. It received FDA 510(k) clearance on 1995-10-06 under 510(k) number K953179. 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 CLM LARYNGOSCOPE?

CLM LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1995-10-06. The listed applicant is Penlon , Ltd.. The 510(k) number is K953179.

When did CLM LARYNGOSCOPE receive FDA 510(k) clearance?

CLM LARYNGOSCOPE received FDA 510(k) clearance on 1995-10-06, under 510(k) number K953179.

Who is the listed applicant for CLM LARYNGOSCOPE?

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

What is the FDA product code for CLM LARYNGOSCOPE?

The FDA product code for CLM LARYNGOSCOPE is CCW.

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Other records listing Penlon , Ltd. 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.

K061102PRIMA ANAESTHESIA MACHINEK041076DELTA TK010318PRIMA OXYGEN MONITORK010317AV 800 VENTILATORK002343SIGMA DELTAK961468QUIK-FIL VAPORIZER KEYED FILLER

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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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