FDA 510(k)

POWER PACK

K-Number: K812440 · 1981-11-02

Decision Date1981-11-02

Product Code

DecisionSubstantially Equivalent

Device Summary

POWER PACK is the device name listed in this FDA 510(k) record. The listed applicant is Black & Decker(Tm). It received FDA 510(k) clearance on 1981-11-02 under 510(k) number K812440. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER PACK?

POWER PACK is a medical device that received FDA 510(k) clearance on 1981-11-02. The listed applicant is Black & Decker(Tm). The 510(k) number is K812440.

When did POWER PACK receive FDA 510(k) clearance?

POWER PACK received FDA 510(k) clearance on 1981-11-02, under 510(k) number K812440.

Who is the listed applicant for POWER PACK?

The FDA 510(k) record lists Black & Decker(Tm) as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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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Other records listing Black & Decker(Tm) as applicant

K820351CAST CUTTER/CAST SAW/INSTRUMENT K812437150 DRIVER REAMER K812436450/800 DRILL K812439DUAL MPC CHARGER K812438SAGITTAL SAW K800314POWER PACK

View all 11 devices →

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.