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FDA 510(k)

NU-BORN BABY BATH KIT

K-Number: K802366 · 1980-10-10

ApplicantAmerican Hospital Supply Corp.
Decision Date1980-10-10
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NU-BORN BABY BATH KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802366. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NU-BORN BABY BATH KIT?

NU-BORN BABY BATH KIT is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K802366.

When did NU-BORN BABY BATH KIT receive FDA 510(k) clearance?

NU-BORN BABY BATH KIT received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802366.

Who is the listed applicant for NU-BORN BABY BATH KIT?

The FDA 510(k) record lists American Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NU-BORN BABY BATH KIT?

The FDA product code for NU-BORN BABY BATH KIT is LDQ.

Other records listing American Hospital Supply Corp. 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.

K854739AMERICAN STERILE SURGICAL ABSORBENT TOWELK854759AMERICAN STERILE MAYO STAND TRAYK832826AAP DOSIMETRY RELEASE OR BASIN SETSK830546DOSIMETRIC RELEASEK822990CONVERTORS PRIMARY WOUND DRESSING IIK830343CONTAINER W/PRIMING SOLUTION

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Related Devices (Code: LDQ)

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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