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FDA 510(k)

MOLLOY INTUBATING STYLETTE

K-Number: K943104 · 1996-04-18

ApplicantMolloy Corp.
Decision Date1996-04-18
Product CodeBSR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOLLOY INTUBATING STYLETTE is the device name listed in this FDA 510(k) record. The listed applicant is Molloy Corp.. It received FDA 510(k) clearance on 1996-04-18 under 510(k) number K943104. The device is classified under product code BSR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOLLOY INTUBATING STYLETTE?

MOLLOY INTUBATING STYLETTE is a medical device that received FDA 510(k) clearance on 1996-04-18. The listed applicant is Molloy Corp.. The 510(k) number is K943104.

When did MOLLOY INTUBATING STYLETTE receive FDA 510(k) clearance?

MOLLOY INTUBATING STYLETTE received FDA 510(k) clearance on 1996-04-18, under 510(k) number K943104.

Who is the listed applicant for MOLLOY INTUBATING STYLETTE?

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

What is the FDA product code for MOLLOY INTUBATING STYLETTE?

The FDA product code for MOLLOY INTUBATING STYLETTE is BSR.

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Related Devices (Code: BSR)

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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