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FDA 510(k)

JOINT MEASUREMENT INDICATOR

K-Number: K861264 · 1986-04-15

ApplicantDevcom, Inc.
Decision Date1986-04-15
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

JOINT MEASUREMENT INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Devcom, Inc.. It received FDA 510(k) clearance on 1986-04-15 under 510(k) number K861264. The device is classified under product code JDL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOINT MEASUREMENT INDICATOR?

JOINT MEASUREMENT INDICATOR is a medical device that received FDA 510(k) clearance on 1986-04-15. The listed applicant is Devcom, Inc.. The 510(k) number is K861264.

When did JOINT MEASUREMENT INDICATOR receive FDA 510(k) clearance?

JOINT MEASUREMENT INDICATOR received FDA 510(k) clearance on 1986-04-15, under 510(k) number K861264.

Who is the listed applicant for JOINT MEASUREMENT INDICATOR?

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 JOINT MEASUREMENT INDICATOR?

The FDA product code for JOINT MEASUREMENT INDICATOR is JDL.

Related Clinical Trials

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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.

K902378CARDIOTHORACIC RULERK874233BLOOD PRESSURE SLEEVE W/TUBINGK863313GRIP STRENGTH DEVICE (GSD)K861043SPINAL EXCURSION METERK850021ELECTROCARDIOGRAPH-ECG CALIPER

Related Devices (Code: JDL)

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.

K073499VERSYS EPOCH FULLCOAT HIP PROSTHESIS, MODEL 4088 SERIESZimmer, Inc.K070785DYNASTY ACETABULAR SYSTEMWrightmedicaltechnologyincK061844DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINERWrightmedicaltechnologyincK051995PROFEMUR RENAISSANCE HIP STEMWrightmedicaltechnologyincK051348CONSERVE TOTAL FEMORAL HEADWrightmedicaltechnologyincK042841M2A/C2A ACETABULAR SYSTEMBiomet, Inc.

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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