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FDA 510(k)

OROPHARYNGEAL SUCTION AIRWAY

K-Number: K770600 · 1977-04-08

ApplicantW.H. Wall, D.D.S.
Decision Date1977-04-08
Product CodeEBR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OROPHARYNGEAL SUCTION AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is W.H. Wall, D.D.S.. It received FDA 510(k) clearance on 1977-04-08 under 510(k) number K770600. The device is classified under product code EBR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OROPHARYNGEAL SUCTION AIRWAY?

OROPHARYNGEAL SUCTION AIRWAY is a medical device that received FDA 510(k) clearance on 1977-04-08. The listed applicant is W.H. Wall, D.D.S.. The 510(k) number is K770600.

When did OROPHARYNGEAL SUCTION AIRWAY receive FDA 510(k) clearance?

OROPHARYNGEAL SUCTION AIRWAY received FDA 510(k) clearance on 1977-04-08, under 510(k) number K770600.

Who is the listed applicant for OROPHARYNGEAL SUCTION AIRWAY?

The FDA 510(k) record lists W.H. Wall, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OROPHARYNGEAL SUCTION AIRWAY?

The FDA product code for OROPHARYNGEAL SUCTION AIRWAY is EBR.

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Related Devices (Code: EBR)

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.

K925367A-DEC 7284 CUSPIDOR, CASCADEA-Dec, Inc.K860058DENPAXNissho Iwai American Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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