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FDA 510(k)

LORRAINE DSL LABOR & DELIVERY BED

K-Number: K842962 · 1984-09-25

ApplicantPulley-Kellam Co., Inc.
Decision Date1984-09-25
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LORRAINE DSL LABOR & DELIVERY BED is the device name listed in this FDA 510(k) record. The listed applicant is Pulley-Kellam Co., Inc.. It received FDA 510(k) clearance on 1984-09-25 under 510(k) number K842962. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LORRAINE DSL LABOR & DELIVERY BED?

LORRAINE DSL LABOR & DELIVERY BED is a medical device that received FDA 510(k) clearance on 1984-09-25. The listed applicant is Pulley-Kellam Co., Inc.. The 510(k) number is K842962.

When did LORRAINE DSL LABOR & DELIVERY BED receive FDA 510(k) clearance?

LORRAINE DSL LABOR & DELIVERY BED received FDA 510(k) clearance on 1984-09-25, under 510(k) number K842962.

Who is the listed applicant for LORRAINE DSL LABOR & DELIVERY BED?

The FDA 510(k) record lists Pulley-Kellam Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LORRAINE DSL LABOR & DELIVERY BED?

The FDA product code for LORRAINE DSL LABOR & DELIVERY BED is KNC.

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Related Devices (Code: KNC)

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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