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FDA 510(k)

MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT

K-Number: K871421 · 1988-01-22

ApplicantFuturemed Div. of Future Impex Corp.
Decision Date1988-01-22
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Futuremed Div. of Future Impex Corp.. It received FDA 510(k) clearance on 1988-01-22 under 510(k) number K871421. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT?

MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT is a medical device that received FDA 510(k) clearance on 1988-01-22. The listed applicant is Futuremed Div. of Future Impex Corp.. The 510(k) number is K871421.

When did MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT receive FDA 510(k) clearance?

MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT received FDA 510(k) clearance on 1988-01-22, under 510(k) number K871421.

Who is the listed applicant for MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT?

The FDA 510(k) record lists Futuremed Div. of Future Impex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT?

The FDA product code for MODEL HL-100 PORTABLE DC ELECT. THERAPEUTIC UNIT is IPF.

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Related Devices (Code: IPF)

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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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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