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FDA 510(k)

MEDISEAL SUCTION CANISTER

K-Number: K895427 · 1990-01-19

ApplicantDeroyal Industries, Inc.
Decision Date1990-01-19
Product CodeDWD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDISEAL SUCTION CANISTER is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1990-01-19 under 510(k) number K895427. The device is classified under product code DWD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISEAL SUCTION CANISTER?

MEDISEAL SUCTION CANISTER is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K895427.

When did MEDISEAL SUCTION CANISTER receive FDA 510(k) clearance?

MEDISEAL SUCTION CANISTER received FDA 510(k) clearance on 1990-01-19, under 510(k) number K895427.

Who is the listed applicant for MEDISEAL SUCTION CANISTER?

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

What is the FDA product code for MEDISEAL SUCTION CANISTER?

The FDA product code for MEDISEAL SUCTION CANISTER is DWD.

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Other records listing Deroyal Industries, Inc. as applicant

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Related Devices (Code: DWD)

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.

K992657IBC VRV, MODEL 1350International Biophysics Corp.K920077NIKKISO NK PUMPInternational Medical Products, Inc.K915481B-D ULTRA-VUE PROCEDURE NEEDLE W/ CHIBA TYPE POINTBd Becton Dickinson Vacutainer Systems PreanalyticK915480B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.Bd Becton Dickinson Vacutainer Systems PreanalyticK915482B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PTBd Becton Dickinson Vacutainer Systems PreanalyticK905311DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.Baxter Bentley Laboratories, 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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