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FDA 510(k)

TURBO 25/30

K-Number: K950256 · 1995-04-04

ApplicantParkell, Inc.
Decision Date1995-04-04
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TURBO 25/30 is the device name listed in this FDA 510(k) record. The listed applicant is Parkell, Inc.. It received FDA 510(k) clearance on 1995-04-04 under 510(k) number K950256. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURBO 25/30?

TURBO 25/30 is a medical device that received FDA 510(k) clearance on 1995-04-04. The listed applicant is Parkell, Inc.. The 510(k) number is K950256.

When did TURBO 25/30 receive FDA 510(k) clearance?

TURBO 25/30 received FDA 510(k) clearance on 1995-04-04, under 510(k) number K950256.

Who is the listed applicant for TURBO 25/30?

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

What is the FDA product code for TURBO 25/30?

The FDA product code for TURBO 25/30 is ELC.

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Related Devices (Code: ELC)

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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