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FDA 510(k)

INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS

K-Number: K875270 · 1988-01-19

ApplicantAir-Shields, Inc.
Decision Date1988-01-19
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS is the device name listed in this FDA 510(k) record. The listed applicant is Air-Shields, Inc.. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K875270. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS?

INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Air-Shields, Inc.. The 510(k) number is K875270.

When did INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS receive FDA 510(k) clearance?

INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS received FDA 510(k) clearance on 1988-01-19, under 510(k) number K875270.

Who is the listed applicant for INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS?

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

What is the FDA product code for INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS?

The FDA product code for INFANT INTENSIVE CARE SYSTEM VERTICAL HEIGHT ADJUS is FMT.

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Other records listing Air-Shields, Inc. as applicant

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Related Devices (Code: FMT)

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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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