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FDA 510(k)

INTERCEPT

K-Number: K843591 · 1984-10-19

ApplicantVital Signs, Inc.
Decision Date1984-10-19
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTERCEPT is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1984-10-19 under 510(k) number K843591. The device is classified under product code KDP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERCEPT?

INTERCEPT is a medical device that received FDA 510(k) clearance on 1984-10-19. The listed applicant is Vital Signs, Inc.. The 510(k) number is K843591.

When did INTERCEPT receive FDA 510(k) clearance?

INTERCEPT received FDA 510(k) clearance on 1984-10-19, under 510(k) number K843591.

Who is the listed applicant for INTERCEPT?

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

What is the FDA product code for INTERCEPT?

The FDA product code for INTERCEPT is KDP.

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Other records listing Vital Signs, Inc. as applicant

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Related Devices (Code: KDP)

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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