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FDA 510(k)

QUINEVAC II

K-Number: K920629 · 1993-03-24

ApplicantRecto Molded Products, Inc.
Decision Date1993-03-24
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

QUINEVAC II is the device name listed in this FDA 510(k) record. The listed applicant is Recto Molded Products, Inc.. It received FDA 510(k) clearance on 1993-03-24 under 510(k) number K920629. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUINEVAC II?

QUINEVAC II is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Recto Molded Products, Inc.. The 510(k) number is K920629.

When did QUINEVAC II receive FDA 510(k) clearance?

QUINEVAC II received FDA 510(k) clearance on 1993-03-24, under 510(k) number K920629.

Who is the listed applicant for QUINEVAC II?

The FDA 510(k) record lists Recto Molded Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUINEVAC II?

The FDA product code for QUINEVAC II is FYD.

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 Recto Molded Products, Inc. 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.

K920628QUINEVAC EVACUATOR/ASPIRATOR

Related Devices (Code: FYD)

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.

K240127PlumeSafe X5 Smoke Management SystemConmed CorporationK2337898Q10 Surclear Smoke Plume Evacuation SystemSurnic CorporationK213068Medline Smoke Evacuation ShroudMedline Industries, Inc.K202944NEBULAE SRS Laparoscopic Surgical Smoke Removal SystemNorthgate Technologies, Inc.K200250Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF SensorMegadyne Medical Products, Inc.K192035EvaQMax Smoke Evacuation SystemBio Protech, 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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