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FDA 510(k)

VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000

K-Number: K875074 · 1988-02-22

ApplicantTimeter Instrument Corp.
Decision Date1988-02-22
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000 is the device name listed in this FDA 510(k) record. The listed applicant is Timeter Instrument Corp.. It received FDA 510(k) clearance on 1988-02-22 under 510(k) number K875074. The device is classified under product code KDP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000?

VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000 is a medical device that received FDA 510(k) clearance on 1988-02-22. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K875074.

When did VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000 receive FDA 510(k) clearance?

VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000 received FDA 510(k) clearance on 1988-02-22, under 510(k) number K875074.

Who is the listed applicant for VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000?

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

What is the FDA product code for VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000?

The FDA product code for VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000 is KDP.

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Other records listing Timeter Instrument 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.

K875075RT-200 COMPUTER INTERFACEK871603CRITERION II & IIA OXYGEN CONCENTRATORSK864836L.A.P. SPIROMETERK834274CRITERION IK823775BORDON GAGE REGULATOR #BGK822746RT-200 CALIBRATION ANALYZER

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Related Devices (Code: KDP)

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.

K013976BOEHRINGER MRI SUCTION REGULATORYBoehringer LaboratoriesK944479PM3300 INTERMITTENT VACUUMPrecision Medical, Inc.K942747MALCOLM-LYNN(TM) EOT SUCTION REG VALVE(TM) (SRV) )Engineered Orthopedic Technologies, Inc.K933232BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIEDBoehringer LaboratoriesK926140VACUUM POWER BODY FLUID SUCTION APPARATUSHill-Rom, Inc.K922817PM3000 & PM3100 VACUUM REGULATORPrecision Medical, 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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