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FDA 510(k)

LITTLE GIANT I & II HANDPIECE CONTROL

K-Number: K801975 · 1980-09-09

ApplicantSilverman'S
Decision Date1980-09-09
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LITTLE GIANT I & II HANDPIECE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Silverman'S. It received FDA 510(k) clearance on 1980-09-09 under 510(k) number K801975. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITTLE GIANT I & II HANDPIECE CONTROL?

LITTLE GIANT I & II HANDPIECE CONTROL is a medical device that received FDA 510(k) clearance on 1980-09-09. The listed applicant is Silverman'S. The 510(k) number is K801975.

When did LITTLE GIANT I & II HANDPIECE CONTROL receive FDA 510(k) clearance?

LITTLE GIANT I & II HANDPIECE CONTROL received FDA 510(k) clearance on 1980-09-09, under 510(k) number K801975.

Who is the listed applicant for LITTLE GIANT I & II HANDPIECE CONTROL?

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

What is the FDA product code for LITTLE GIANT I & II HANDPIECE CONTROL?

The FDA product code for LITTLE GIANT I & II HANDPIECE CONTROL is EIA.

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Other records listing Silverman'S 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.

K831824DENTAL ELECTRONIC/S.B.R TRADING BU HAND

Related Devices (Code: EIA)

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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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