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FDA 510(k)

DATASCRIBE #DS-40

K-Number: K812765 · 1981-11-16

ApplicantTimeter Instrument Corp.
Decision Date1981-11-16
Product CodeBXW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DATASCRIBE #DS-40 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 1981-11-16 under 510(k) number K812765. The device is classified under product code BXW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATASCRIBE #DS-40?

DATASCRIBE #DS-40 is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K812765.

When did DATASCRIBE #DS-40 receive FDA 510(k) clearance?

DATASCRIBE #DS-40 received FDA 510(k) clearance on 1981-11-16, under 510(k) number K812765.

Who is the listed applicant for DATASCRIBE #DS-40?

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 DATASCRIBE #DS-40?

The FDA product code for DATASCRIBE #DS-40 is BXW.

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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: BXW)

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K853848RESPIRATORY DIAGNOSTIC EQUIPMENT CALIBRATORMedical Graphics Corp.K831758FLOW-CALIBRATION MODULEThe Perkin-Elmer Corp.K830898SYRINGE 500BC BE #7000Instrumentation Industries, Inc.K810290OHIO CAL-CHEKOhio Medical ProductsK760520CALIPERS, MCGAW SKINFOLDMcgaw Laboratories

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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