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FDA 510(k)

OHMEDA CONTINUOUS SUCTION REGULATOR

K-Number: K883229 · 1988-10-19

ApplicantOhmeda Medical
Decision Date1988-10-19
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OHMEDA CONTINUOUS SUCTION REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1988-10-19 under 510(k) number K883229. 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 OHMEDA CONTINUOUS SUCTION REGULATOR?

OHMEDA CONTINUOUS SUCTION REGULATOR is a medical device that received FDA 510(k) clearance on 1988-10-19. The listed applicant is Ohmeda Medical. The 510(k) number is K883229.

When did OHMEDA CONTINUOUS SUCTION REGULATOR receive FDA 510(k) clearance?

OHMEDA CONTINUOUS SUCTION REGULATOR received FDA 510(k) clearance on 1988-10-19, under 510(k) number K883229.

Who is the listed applicant for OHMEDA CONTINUOUS SUCTION REGULATOR?

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

What is the FDA product code for OHMEDA CONTINUOUS SUCTION REGULATOR?

The FDA product code for OHMEDA CONTINUOUS SUCTION REGULATOR is KDP.

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Other records listing Ohmeda Medical 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.

K123309GIRAFFE AND PANDA WARMERSK101788GIRAFFE OMNIBEDK101778GIRAFFE INCUBATORK090697MODIFICATION TO: GIRAFFE AND PANDA WARMERK072157MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)K070377GIRAFFE AND PANDA WARMER

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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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