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FDA 510(k)

CARDIOTHORACIC RULER

K-Number: K902378 · 1990-06-14

ApplicantDevcom, Inc.
Decision Date1990-06-14
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARDIOTHORACIC RULER is the device name listed in this FDA 510(k) record. The listed applicant is Devcom, Inc.. It received FDA 510(k) clearance on 1990-06-14 under 510(k) number K902378. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOTHORACIC RULER?

CARDIOTHORACIC RULER is a medical device that received FDA 510(k) clearance on 1990-06-14. The listed applicant is Devcom, Inc.. The 510(k) number is K902378.

When did CARDIOTHORACIC RULER receive FDA 510(k) clearance?

CARDIOTHORACIC RULER received FDA 510(k) clearance on 1990-06-14, under 510(k) number K902378.

Who is the listed applicant for CARDIOTHORACIC RULER?

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

What is the FDA product code for CARDIOTHORACIC RULER?

The FDA product code for CARDIOTHORACIC RULER is KPR.

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Other records listing Devcom, Inc. 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.

K874233BLOOD PRESSURE SLEEVE W/TUBINGK863313GRIP STRENGTH DEVICE (GSD)K861264JOINT MEASUREMENT INDICATORK861043SPINAL EXCURSION METERK850021ELECTROCARDIOGRAPH-ECG CALIPER

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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