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FDA 510(k)

MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS

K-Number: K884165 · 1988-10-26

ApplicantSpark Instruments & Academics, Inc.
Decision Date1988-10-26
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS is the device name listed in this FDA 510(k) record. The listed applicant is Spark Instruments & Academics, Inc.. It received FDA 510(k) clearance on 1988-10-26 under 510(k) number K884165. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS?

MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS is a medical device that received FDA 510(k) clearance on 1988-10-26. The listed applicant is Spark Instruments & Academics, Inc.. The 510(k) number is K884165.

When did MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS receive FDA 510(k) clearance?

MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS received FDA 510(k) clearance on 1988-10-26, under 510(k) number K884165.

Who is the listed applicant for MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS?

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

What is the FDA product code for MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS?

The FDA product code for MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS is LBB.

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Other records listing Spark Instruments & Academics, 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.

K861396HANDHELD DYNAMOMETER, MODEL #160 AND #111

Related Devices (Code: LBB)

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.

K162412Hoggan Scientific® microFET2™Hoggan Scientific, LLCK073154FACTS HAND AND PINCH GRIP COMBOGlobal Services Group, LLCK052309DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006Saehan Corp.K042889DYNAMOMETER - MODEL FCE AND MODEL MSCAmetekK012492KADANCE 2000Kada Research, Inc.K981730DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002Nk Biotechnical Corp.

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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