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FDA 510(k)

MECK/MILLER VENTILATION TUBE HARNESS

K-Number: K760993 · 1976-12-09

ApplicantTimeter Instrument Corp.
Decision Date1976-12-09
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MECK/MILLER VENTILATION TUBE HARNESS 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 1976-12-09 under 510(k) number K760993. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MECK/MILLER VENTILATION TUBE HARNESS?

MECK/MILLER VENTILATION TUBE HARNESS is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K760993.

When did MECK/MILLER VENTILATION TUBE HARNESS receive FDA 510(k) clearance?

MECK/MILLER VENTILATION TUBE HARNESS received FDA 510(k) clearance on 1976-12-09, under 510(k) number K760993.

Who is the listed applicant for MECK/MILLER VENTILATION TUBE HARNESS?

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 MECK/MILLER VENTILATION TUBE HARNESS?

The FDA product code for MECK/MILLER VENTILATION TUBE HARNESS is BZO.

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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 INTERFACEK875074VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000K871603CRITERION II & IIA OXYGEN CONCENTRATORSK864836L.A.P. SPIROMETERK834274CRITERION IK823775BORDON GAGE REGULATOR #BG

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Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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