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FDA 510(k)

MEDI PUMP ASPIRATOR MODELS 1130 AND 1135

K-Number: K952806 · 1995-10-26

Decision Date1995-10-26
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDI PUMP ASPIRATOR MODELS 1130 AND 1135 is the device name listed in this FDA 510(k) record. The listed applicant is Thomas Industries. It received FDA 510(k) clearance on 1995-10-26 under 510(k) number K952806. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI PUMP ASPIRATOR MODELS 1130 AND 1135?

MEDI PUMP ASPIRATOR MODELS 1130 AND 1135 is a medical device that received FDA 510(k) clearance on 1995-10-26. The listed applicant is Thomas Industries. The 510(k) number is K952806.

When did MEDI PUMP ASPIRATOR MODELS 1130 AND 1135 receive FDA 510(k) clearance?

MEDI PUMP ASPIRATOR MODELS 1130 AND 1135 received FDA 510(k) clearance on 1995-10-26, under 510(k) number K952806.

Who is the listed applicant for MEDI PUMP ASPIRATOR MODELS 1130 AND 1135?

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

What is the FDA product code for MEDI PUMP ASPIRATOR MODELS 1130 AND 1135?

The FDA product code for MEDI PUMP ASPIRATOR MODELS 1130 AND 1135 is BTA.

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 Thomas Industries 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 9 devices →

Related Devices (Code: BTA)

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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