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FDA 510(k)

DISS FEMALE AIR ADAPTOR

K-Number: K813235 · 1981-12-08

ApplicantTimeter Instrument Corp.
Decision Date1981-12-08
Product CodeBYK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISS FEMALE AIR ADAPTOR 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 1981-12-08 under 510(k) number K813235. The device is classified under product code BYK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISS FEMALE AIR ADAPTOR?

DISS FEMALE AIR ADAPTOR is a medical device that received FDA 510(k) clearance on 1981-12-08. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K813235.

When did DISS FEMALE AIR ADAPTOR receive FDA 510(k) clearance?

DISS FEMALE AIR ADAPTOR received FDA 510(k) clearance on 1981-12-08, under 510(k) number K813235.

Who is the listed applicant for DISS FEMALE AIR ADAPTOR?

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 DISS FEMALE AIR ADAPTOR?

The FDA product code for DISS FEMALE AIR ADAPTOR is BYK.

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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: BYK)

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.

K941547CAM 4 THERMOELECTRIC CHILD/ADULT MIST TENTAllied Healthcare Products, Inc.K882817LUNG DIFFUSION GAS MIXTURESwisco, 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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