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FDA 510(k)

IBC VRV, MODEL 1350

K-Number: K992657 · 2000-02-18

ApplicantInternational Biophysics Corp.
Decision Date2000-02-18
Product CodeDWD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IBC VRV, MODEL 1350 is the device name listed in this FDA 510(k) record. The listed applicant is International Biophysics Corp.. It received FDA 510(k) clearance on 2000-02-18 under 510(k) number K992657. 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 IBC VRV, MODEL 1350?

IBC VRV, MODEL 1350 is a medical device that received FDA 510(k) clearance on 2000-02-18. The listed applicant is International Biophysics Corp.. The 510(k) number is K992657.

When did IBC VRV, MODEL 1350 receive FDA 510(k) clearance?

IBC VRV, MODEL 1350 received FDA 510(k) clearance on 2000-02-18, under 510(k) number K992657.

Who is the listed applicant for IBC VRV, MODEL 1350?

The FDA 510(k) record lists International Biophysics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IBC VRV, MODEL 1350?

The FDA product code for IBC VRV, MODEL 1350 is DWD.

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Other records listing International Biophysics Corp. 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.

K072688LIFECHOICE OXYGEN CONCENTRATOR, MODEL OXY1000K030181INTERNATIONAL BIOPHYSICS CORPORATION (IBC) LASER PEEL SYSTEMK992785IBC FLOGUARD, MODEL 6050K992964IBC VENT VALVE, MODEL 1400K983272IBC FLOPUMP, MODEL 6000K963703ACCUFLO MONITORING SYSTEM (1800)/ ACCUFLO PROBE (8000)

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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.

K920077NIKKISO NK PUMPInternational Medical Products, Inc.K915482B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PTBd Becton Dickinson Vacutainer Systems PreanalyticK915481B-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 PreanalyticK905311DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.Baxter Bentley Laboratories, Inc.K895427MEDISEAL SUCTION CANISTERDeroyal Industries, 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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