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FDA 510(k)

NEONATAL BLOOD COLLECTION AND SCREENING FORM

K-Number: K944618 · 1995-05-10

ApplicantGeneral Business Forms, Inc.
Decision Date1995-05-10
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NEONATAL BLOOD COLLECTION AND SCREENING FORM is the device name listed in this FDA 510(k) record. The listed applicant is General Business Forms, Inc.. It received FDA 510(k) clearance on 1995-05-10 under 510(k) number K944618. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEONATAL BLOOD COLLECTION AND SCREENING FORM?

NEONATAL BLOOD COLLECTION AND SCREENING FORM is a medical device that received FDA 510(k) clearance on 1995-05-10. The listed applicant is General Business Forms, Inc.. The 510(k) number is K944618.

When did NEONATAL BLOOD COLLECTION AND SCREENING FORM receive FDA 510(k) clearance?

NEONATAL BLOOD COLLECTION AND SCREENING FORM received FDA 510(k) clearance on 1995-05-10, under 510(k) number K944618.

Who is the listed applicant for NEONATAL BLOOD COLLECTION AND SCREENING FORM?

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

What is the FDA product code for NEONATAL BLOOD COLLECTION AND SCREENING FORM?

The FDA product code for NEONATAL BLOOD COLLECTION AND SCREENING FORM is JKA.

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Related Devices (Code: JKA)

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

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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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