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FDA 510(k)

TENSION-ISOMETER

K-Number: K854254 · 1985-11-15

ApplicantMedmetric Corp.
Decision Date1985-11-15
Product CodeLXI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TENSION-ISOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medmetric Corp.. It received FDA 510(k) clearance on 1985-11-15 under 510(k) number K854254. The device is classified under product code LXI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TENSION-ISOMETER?

TENSION-ISOMETER is a medical device that received FDA 510(k) clearance on 1985-11-15. The listed applicant is Medmetric Corp.. The 510(k) number is K854254.

When did TENSION-ISOMETER receive FDA 510(k) clearance?

TENSION-ISOMETER received FDA 510(k) clearance on 1985-11-15, under 510(k) number K854254.

Who is the listed applicant for TENSION-ISOMETER?

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

What is the FDA product code for TENSION-ISOMETER?

The FDA product code for TENSION-ISOMETER is LXI.

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Other records listing Medmetric 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.

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Related Devices (Code: LXI)

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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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