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FDA 510(k)

ANTI-CONVULSANT DRUG CONTROL

K-Number: K770975 · 1977-06-08

ApplicantLederle Laboratories
Decision Date1977-06-08
Product CodeDIC
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ANTI-CONVULSANT DRUG CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Lederle Laboratories. It received FDA 510(k) clearance on 1977-06-08 under 510(k) number K770975. The device is classified under product code DIC. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTI-CONVULSANT DRUG CONTROL?

ANTI-CONVULSANT DRUG CONTROL is a medical device that received FDA 510(k) clearance on 1977-06-08. The listed applicant is Lederle Laboratories. The 510(k) number is K770975.

When did ANTI-CONVULSANT DRUG CONTROL receive FDA 510(k) clearance?

ANTI-CONVULSANT DRUG CONTROL received FDA 510(k) clearance on 1977-06-08, under 510(k) number K770975.

Who is the listed applicant for ANTI-CONVULSANT DRUG CONTROL?

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

What is the FDA product code for ANTI-CONVULSANT DRUG CONTROL?

The FDA product code for ANTI-CONVULSANT DRUG CONTROL is DIC.

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Other records listing Lederle Laboratories 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.

K770307MICRO/PETTOR, SMIK760467ROTATOR, FIXED SPEED

Related Devices (Code: DIC)

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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