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FDA 510(k)

NASAL E.T. TAPE

K-Number: K900787 · 1990-03-16

Decision Date1990-03-16
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NASAL E.T. TAPE is the device name listed in this FDA 510(k) record. The listed applicant is B&B Medical Technologies, Inc.. It received FDA 510(k) clearance on 1990-03-16 under 510(k) number K900787. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NASAL E.T. TAPE?

NASAL E.T. TAPE is a medical device that received FDA 510(k) clearance on 1990-03-16. The listed applicant is B&B Medical Technologies, Inc.. The 510(k) number is K900787.

When did NASAL E.T. TAPE receive FDA 510(k) clearance?

NASAL E.T. TAPE received FDA 510(k) clearance on 1990-03-16, under 510(k) number K900787.

Who is the listed applicant for NASAL E.T. TAPE?

The FDA 510(k) record lists B&B Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NASAL E.T. TAPE?

The FDA product code for NASAL E.T. TAPE is CBH.

Related Clinical Trials

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.

Other records listing B&B Medical Technologies, Inc. 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.

View all 23 devices →

Related Devices (Code: CBH)

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.

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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