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FDA 510(k)

E.T. PUFFER

K-Number: K884374 · 1988-11-23

ApplicantKalajian Ent.
Decision Date1988-11-23
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

E.T. PUFFER is the device name listed in this FDA 510(k) record. The listed applicant is Kalajian Ent.. It received FDA 510(k) clearance on 1988-11-23 under 510(k) number K884374. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E.T. PUFFER?

E.T. PUFFER is a medical device that received FDA 510(k) clearance on 1988-11-23. The listed applicant is Kalajian Ent.. The 510(k) number is K884374.

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

E.T. PUFFER received FDA 510(k) clearance on 1988-11-23, under 510(k) number K884374.

Who is the listed applicant for E.T. PUFFER?

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

What is the FDA product code for E.T. PUFFER?

The FDA product code for E.T. PUFFER is BZA.

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.

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Other records listing Kalajian Ent. 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.

K883902INFUSA-PLATEK870600SOFT EAR STETHOSCOPE

Related Devices (Code: BZA)

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.

K083702TRACH-ASSISTMergenet MedicalK954383SURELOC CIRCUIT CONNECTORPolamedco, Inc.K954197DISPOSABLE FLEX TUBEEngstrom MedicalK953786UNICOR, INC. CONNECTORS & AIRWAY EXTENSIONSUnicor, Inc.K952824NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTORIntertex Medical, Inc.K951345DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLINGCatheter Research, Inc.

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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