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FDA 510(k)

PILLING IDENTI-LOOPS

K-Number: K820377 · 1982-03-10

ApplicantNarco Scientific
Decision Date1982-03-10
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PILLING IDENTI-LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1982-03-10 under 510(k) number K820377. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLING IDENTI-LOOPS?

PILLING IDENTI-LOOPS is a medical device that received FDA 510(k) clearance on 1982-03-10. The listed applicant is Narco Scientific. The 510(k) number is K820377.

When did PILLING IDENTI-LOOPS receive FDA 510(k) clearance?

PILLING IDENTI-LOOPS received FDA 510(k) clearance on 1982-03-10, under 510(k) number K820377.

Who is the listed applicant for PILLING IDENTI-LOOPS?

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

What is the FDA product code for PILLING IDENTI-LOOPS?

The FDA product code for PILLING IDENTI-LOOPS is GAD.

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Other records listing Narco Scientific 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.

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Related Devices (Code: GAD)

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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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